Month: October 2022

Ethers lack the hydroxyl groups of alcohols. Without the strongly polarized O―H bond, ether molecules cannot engage in hydrogen bonding with each other. 38256-93-8, formula is C4H11NO, Name is 2-Methoxy-N-methylethanamine. Ethers do have nonbonding electron pairs on their oxygen atoms, however, and they can form hydrogen bonds with other molecules (alcohols, amines, etc.) that have O―H or N―H bonds. Recommanded Product: 2-Methoxy-N-methylethanamine.

Mohamad, Rapidah;Awang, Normah;FarahanaKamaludin, Nurul research published 《 Synthesis and characterization of new organotin (IV)(2-Methoxyethyl)- methyldithiocarbamate complexes》, the research content is summarized as follows. Three new organotin(IV) dithiocarbamate complexes (complexes 1-3) employing (2-methoxyethyl)-methylamine as their secondary amine were successfully synthesized in situ. Elemental anal. of the complexes gave the general formula of RnSn[S2CN(C2H4OCH3)(CH3)]n-2 where R = C4H9(Bu) and C6H5Phfor n = 2; R = C6H11 (Cy) for n = 3. The complexes were analyzed using FTIR and 1H, 13C, and 119Sn NMR. The important absorption peaks and chem. shift of NCS2 carbon were found in all the three complexes. 119Sn NMR suggested that tin atom in the complexes are coordinated by five and six coordination numbers

38256-93-8, 2-Methoxy-N-methylethanamine is a useful research compound. Its molecular formula is C4H11NO and its molecular weight is 89.14 g/mol. The purity is usually 95%.
2-Methoxy-N-methylethanamine is a drug that binds to the cannabinoid receptor CB1. It has been shown to be effective in the treatment of cardiac arrhythmia and may also be used as an anti-inflammatory drug. 2MEMEA has been shown to have pharmacokinetic properties that are different from those of other amines, which may be due to its ability to form hydrogen bonds with water molecules. 2MEMEA also has diversified effects on some types of cancer cells, including hyperproliferative and amine-dependent cancers., Recommanded Product: 2-Methoxy-N-methylethanamine

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Ethers are a class of organic compounds that contain an ether group—an oxygen atom connected to two alkyl or aryl groups. 38256-93-8, formula is C4H11NO, Name is 2-Methoxy-N-methylethanamine.They have the general formula R–O–R′, where R and R′ represent the alkyl or aryl groups. COA of Formula: C4H11NO.

Mohamad, Rapidah;Awang, Normah;Kamaludin, Nurul Farahana;Pim, Norraphat Uttraphan research published 《 Spectral characterization and X-Ray crystallographic studies of some triphenyltin(IV) dithiocarbamates compounds》, the research content is summarized as follows. Three novel triphenyltin(IV) compounds with N-(2-methoxyethyl)-N-methyldithiocarbamate (1), N-benzyl-N-phenethyldithiocarbamate (2) and N-methyl-N-hexyldithiocarbamate (3) ligands have been successfully synthesized via in situ insertion method. The newly synthesized compounds gave fairly sharp m.ps. indicating their purity and were successfully isolated as crystalline solids. All the compounds have been characterized by CHNS elemental anal., FT-IR, ¹H, ¹³C and ¹¹⁹Sn NMR spectroscopies. A single C-S vibration band around 1000cm^-1 was observed in all compounds, suggesting bidentate bonding of dithiocarbamate ligand to tin metal through both sulfur donor atoms. The crystal structures of all the compounds were determined by x-ray crystallog. All the compounds were crystallized in triclinic system. The single crystal x-ray diffraction data illustrated all three dithiocarbamato ligands are bidentate but in asym. fashion due to D (Sn-S) bond length and the geometry at the tin center is described as distorted trigonal bipyramidal.

COA of Formula: C4H11NO, 2-Methoxy-N-methylethanamine is a useful research compound. Its molecular formula is C4H11NO and its molecular weight is 89.14 g/mol. The purity is usually 95%.
2-Methoxy-N-methylethanamine is a drug that binds to the cannabinoid receptor CB1. It has been shown to be effective in the treatment of cardiac arrhythmia and may also be used as an anti-inflammatory drug. 2MEMEA has been shown to have pharmacokinetic properties that are different from those of other amines, which may be due to its ability to form hydrogen bonds with water molecules. 2MEMEA also has diversified effects on some types of cancer cells, including hyperproliferative and amine-dependent cancers., 38256-93-8.

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Ethers do have nonbonding electron pairs on their oxygen atoms, 38256-93-8, formula is C4H11NO, Name is 2-Methoxy-N-methylethanamine. The ability to form hydrogen bonds with other compounds makes ethers particularly good solvents for a wide variety of organic compounds and a surprisingly large number of inorganic compounds. Application In Synthesis of 38256-93-8.

Mohamad, Rapidah;Awang, Normah;Kamaludin, Nurul Farahana;Jotani, Mukesh M.;Tiekink, Edward R. T. research published 《 Crystal structures and Hirshfeld surface analyses of bis[N,N-bis(2-methoxyethyl)dithiocarbamato-κ²S,S’]di-n-butyltin(IV) and [N-(2-methoxyethyl)-N-methyldithiocarbamato-κ²S,S’]triphenyltin(IV)》, the research content is summarized as follows. The crystal and mol. structures of the two title organotin dithiocarbamate compounds, [Sn(C₄H₉)₂(C₇H₁₄NO₂S₂)₂], (I), and [Sn(C₆H₅)₃(C₅H₁₀NOS₂)], (II), are described. Both structures feature asym. bound dithiocarbamate ligands leading to a skew-trapezoidal bipyramidal geometry for the metal atom in (I) and a distorted tetrahedral geometry in (II). The complete mol. of (I) is generated by a crystallog. twofold axis (Sn site symmetry 2). In the crystal of (I), mols. self-assemble into a supramol. array parallel to (10-1) via methylene-C-H···O(methoxy) interactions. In the crystal of (II), supramol. dimers are formed via pairs of weak phenyl-C-H···π(phenyl) contacts. In each of (I) and (II), the specified assemblies connect into a three-dimensional architecture without directional interactions between them. Hirshfeld surface analyses confirm the importance of H···H contacts in the mol. packing of each of (I) and (II), and in the case of (I), highlight the importance of short methoxy-H···H(butyl) contacts between layers.

Application In Synthesis of 38256-93-8, 2-Methoxy-N-methylethanamine is a useful research compound. Its molecular formula is C4H11NO and its molecular weight is 89.14 g/mol. The purity is usually 95%.
2-Methoxy-N-methylethanamine is a drug that binds to the cannabinoid receptor CB1. It has been shown to be effective in the treatment of cardiac arrhythmia and may also be used as an anti-inflammatory drug. 2MEMEA has been shown to have pharmacokinetic properties that are different from those of other amines, which may be due to its ability to form hydrogen bonds with water molecules. 2MEMEA also has diversified effects on some types of cancer cells, including hyperproliferative and amine-dependent cancers., 38256-93-8.

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Ethers feature bent C–O–C linkages. In dimethyl ether, the bond angle is 111° and C–O distances are 141 pm. 38256-93-8, formula is C4H11NO, Name is 2-Methoxy-N-methylethanamine. The barrier to rotation about the C–O bonds is low. The bonding of oxygen in ethers, alcohols, and water is similar. In the language of valence bond theory, the hybridization at oxygen is sp3. Safety of 2-Methoxy-N-methylethanamine.

Mohamad, Rapidah;Awang, Normah;Kamaludin, Nurul F.;Jotani, Mukesh M.;Tiekink, Edward R. T. research published 《 Di-n-butylbis[N-(2-methoxyethyl)-N-methyldithiocarbamato-κ²S,S′]tin(IV): crystal structure and Hirshfeld surface analysis》, the research content is summarized as follows. The complete mol. of the title compound, [Sn(C₄H₉)₂(C₅H₁₀NOS₂)₂], is generated by a crystallog. mirror plane, with the Sn^IV atom and the two inner methylene C atoms of the Bu ligands lying on the mirror plane; statistical disorder is noted in the two terminal Et groups, which deviate from mirror symmetry. The dithiocarbamate ligand coordinates to the metal atom in an asym. mode with the resulting C₂S₄ donor set defining a skew trapezoidal bipyramidal geometry; the Bu groups are disposed to lie over the longer Sn-S bonds. Supramol. chains aligned along the a-axis direction and sustained by methylene-C-H···S(weakly coordinating) interactions feature in the mol. packing. A Hirshfeld surface anal. reveals the dominance of H···H contacts in the crystal.

Safety of 2-Methoxy-N-methylethanamine, 2-Methoxy-N-methylethanamine is a useful research compound. Its molecular formula is C4H11NO and its molecular weight is 89.14 g/mol. The purity is usually 95%.
2-Methoxy-N-methylethanamine is a drug that binds to the cannabinoid receptor CB1. It has been shown to be effective in the treatment of cardiac arrhythmia and may also be used as an anti-inflammatory drug. 2MEMEA has been shown to have pharmacokinetic properties that are different from those of other amines, which may be due to its ability to form hydrogen bonds with water molecules. 2MEMEA also has diversified effects on some types of cancer cells, including hyperproliferative and amine-dependent cancers., 38256-93-8.

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Ethers are a class of organic compounds that contain an ether group—an oxygen atom connected to two alkyl or aryl groups. 38256-93-8, formula is C4H11NO, Name is 2-Methoxy-N-methylethanamine.They have the general formula R–O–R′, where R and R′ represent the alkyl or aryl groups. Name: 2-Methoxy-N-methylethanamine.

Mohamad, Rapidah;Awang, Normah;Jotani, Mukesh M.;Tiekink, Edward R. T. research published 《 Distinct coordination geometries in bis[N,N-bis(2-methoxyethyl)dithiocarbamato-κ²S,S′]diphenyltin(IV) and bis[N-(2-methoxyethyl)-N-methyldithiocarbamato-κ²S,S′]diphenyltin(IV): crystal structures and Hirshfeld surface analysis》, the research content is summarized as follows. The crystal and mol. structures of two diphenyltin bis(dithiocarbamate)s, [Sn(C₆H₅)₂(C₅H₁₀NOS₂)₂], (I), and [Sn(C₆H₅)₂(C₇H₁₄NO₂S₂)₂], (II), are described. In (I), in which the metal atom lies on a twofold rotation axis, the dithiocarbamate ligand coordinates with approx. equal Sn-S bond lengths and the ipso-C atoms of the Sn-bound Ph groups occupy cis-positions in the resulting octahedral C₂S₄ donor set. A quite distinct coordination geometry is noted in (II), arising as a result of quite disparate Sn-S bond lengths. Here, the four S-donors define a trapezoidal plane with the ipso-C atoms lying over the weaker of the Sn-S bonds so that the C₂S₄ donor set defines a skewed trapezoidal bipyramid. The packing of (I) features supramol. layers in the ab plane sustained by methylene-C-H···π(Sn-aryl) interactions. In (II), supramol. chains along the b-axis direction are formed by methylene-C-O(ether) interactions; these pack with no directional interactions between them. A Hirshfeld surface anal. was conducted on both (I) and (II) and revealed the dominance of H···H interactions contributing to the resp. surfaces, i.e. >60% in each case, and other features consistent with the description of the mol. packing above.

38256-93-8, 2-Methoxy-N-methylethanamine is a useful research compound. Its molecular formula is C4H11NO and its molecular weight is 89.14 g/mol. The purity is usually 95%.
2-Methoxy-N-methylethanamine is a drug that binds to the cannabinoid receptor CB1. It has been shown to be effective in the treatment of cardiac arrhythmia and may also be used as an anti-inflammatory drug. 2MEMEA has been shown to have pharmacokinetic properties that are different from those of other amines, which may be due to its ability to form hydrogen bonds with water molecules. 2MEMEA also has diversified effects on some types of cancer cells, including hyperproliferative and amine-dependent cancers., Name: 2-Methoxy-N-methylethanamine

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Ethers lack the hydroxyl groups of alcohols. Without the strongly polarized O―H bond, ether molecules cannot engage in hydrogen bonding with each other. 38256-93-8, formula is C4H11NO, Name is 2-Methoxy-N-methylethanamine. Ethers do have nonbonding electron pairs on their oxygen atoms, however, and they can form hydrogen bonds with other molecules (alcohols, amines, etc.) that have O―H or N―H bonds. Safety of 2-Methoxy-N-methylethanamine.

Miyazaki, Masaki;Naito, Hiroyuki;Sugimoto, Yuuichi;Kawato, Haruko;Okayama, Tooru;Shimizu, Hironari;Miyazaki, Masaya;Kitagawa, Mayumi;Seki, Takahiko;Fukutake, Setsuko;Aonuma, Masashi;Soga, Tsunehiko research published 《 Lead optimization of novel p53-MDM2 interaction inhibitors possessing dihydroimidazothiazole scaffold》, the research content is summarized as follows. With the aim of discovering potent inhibitors of the p53-MDM2 interaction and thus obtaining a potent anticancer drug, we have pursued synthesis and optimization of dihydroimidazothiazole derivatives, which have been discovered via scaffold hopping by mimicking the mode of interaction between MDM2 and Nutlins. Upon the discovery we encountered a problem involving the chem. instability of the scaffold, i.e., susceptibility to oxidation which led to imidazothiazole. In order to solve this problem and to obtain further potent compounds, we executed medicinal research and thus furnished the optimal compounds by incorporating the Me group onto the C-6 position to avoid the oxidation, and by modifying the C-2 moiety of the addnl. proline motif, which furnished high potency. The incorporation of the pyrrolidine moiety at the C-2 position raised another hydrophobic interaction site with MDM2 protein, which was generated by the induced-fitting observed by co-crystal structure anal. These optimal mols. showed significant improvement in potency when compared with the early leads.

38256-93-8, 2-Methoxy-N-methylethanamine is a useful research compound. Its molecular formula is C4H11NO and its molecular weight is 89.14 g/mol. The purity is usually 95%.
2-Methoxy-N-methylethanamine is a drug that binds to the cannabinoid receptor CB1. It has been shown to be effective in the treatment of cardiac arrhythmia and may also be used as an anti-inflammatory drug. 2MEMEA has been shown to have pharmacokinetic properties that are different from those of other amines, which may be due to its ability to form hydrogen bonds with water molecules. 2MEMEA also has diversified effects on some types of cancer cells, including hyperproliferative and amine-dependent cancers., Safety of 2-Methoxy-N-methylethanamine

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Ethers lack the hydroxyl groups of alcohols. Without the strongly polarized O―H bond, ether molecules cannot engage in hydrogen bonding with each other. 38256-93-8, formula is C4H11NO, Name is 2-Methoxy-N-methylethanamine. Ethers do have nonbonding electron pairs on their oxygen atoms, however, and they can form hydrogen bonds with other molecules (alcohols, amines, etc.) that have O―H or N―H bonds. Name: 2-Methoxy-N-methylethanamine.

Miwa, Kazuhiro;Hitaka, Takenori;Imada, Takashi;Sasaki, Satoshi;Yoshimatsu, Mie;Kusaka, Masami;Tanaka, Akira;Nakata, Daisuke;Furuya, Shuichi;Endo, Satoshi;Hamamura, Kazumasa;Kitazaki, Tomoyuki research published 《 Discovery of 1-{4-[1-(2,6-Difluorobenzyl)-5-[(dimethylamino)methyl]-3-(6-methoxypyridazin-3-yl)-2,4-dioxo-1,2,3,4-tetrahydrothieno[2,3-d]pyrimidin-6-yl]phenyl}-3-methoxyurea (TAK-385) as a Potent, Orally Active, Non-Peptide Antagonist of the Human Gonadotropin-Releasing Hormone Receptor》, the research content is summarized as follows. An orally active human gonadotropin-releasing hormone (GnRH) receptor antagonist, thieno[2,3-d]pyrimidine-2,4-dione derivative I (sufugolix), was previously discovered. To reduce the cytochrome P 450 (CYP) inhibitory activity and improve in vivo GnRH antagonistic activity, further optimization of this scaffold was carried out. The synthetic efforts were focused on chem. modification at the 5 and 3 positions of the thieno[2,3-d]pyrimidine-2,4-dione ring based on computational modeling, which resulted in the discovery of 1-{4-[1-(2,6-difluorobenzyl)-5-[(dimethylamino)methyl]-3-(6-methoxypyridazin-3-yl)-2,4-dioxo-1,2,3,4-tetrahydrothieno[2,3-d]pyrimidin-6-yl]phenyl}-3-methoxyurea (II) as a highly potent and orally active GnRH antagonist. Compound II showed potent in vitro GnRH antagonistic activity in the presence of fetal bovine serum (FBS) without CYP inhibition. Oral administration of II maintained the suppressive effect of the plasma LH levels in castrated cynomolgus monkeys at a 3 mg/kg dose for more than 24 h. Compound II is currently under clin. development with the code name of TAK-385.

Name: 2-Methoxy-N-methylethanamine, 2-Methoxy-N-methylethanamine is a useful research compound. Its molecular formula is C4H11NO and its molecular weight is 89.14 g/mol. The purity is usually 95%.
2-Methoxy-N-methylethanamine is a drug that binds to the cannabinoid receptor CB1. It has been shown to be effective in the treatment of cardiac arrhythmia and may also be used as an anti-inflammatory drug. 2MEMEA has been shown to have pharmacokinetic properties that are different from those of other amines, which may be due to its ability to form hydrogen bonds with water molecules. 2MEMEA also has diversified effects on some types of cancer cells, including hyperproliferative and amine-dependent cancers., 38256-93-8.

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Ethers feature bent C–O–C linkages. In dimethyl ether, the bond angle is 111° and C–O distances are 141 pm. 111-90-0, formula is C6H14O3, Name is Diethylene Glycol Monoethyl Ether. The barrier to rotation about the C–O bonds is low. The bonding of oxygen in ethers, alcohols, and water is similar. In the language of valence bond theory, the hybridization at oxygen is sp3. Reference of 111-90-0.

Mittal, Saurabh;Ali, Javed;Baboota, Sanjula research published 《 Enhanced anti-psoriatic activity of tacrolimus loaded nanoemulsion gel via omega 3 – Fatty acid (EPA and DHA) rich oils-fish oil and linseed oil》, the research content is summarized as follows. Psoriasis is an autoimmune disease that affects around 3-4% of the population globally leading to skin inflammation. Tacrolimus is widely used in the treatment of psoriasis due to its ability to suppress inflammation and immune response. But formation of scaly plaques and dry patches are hurdle in delivering drug via topical route. The aim of present study was to develop, optimize and characterize tacrolimus loaded nanoemulsion gel to get enhanced anti-psoriatic activity. Nanoemulsion was prepared using spontaneous emulsification method combined with high pressure homogenization technique using fish oil and linseed oil (2 different oils), tween 80 (surfactant) and transcutol-P (co-surfactant). Fish oil and linseed oil were used as oil phase as they contain high amount of eicosapentaenoic acid and docosahexaenoic acid, and possess anti-inflammatory activity. The optimized nanoemulsions (fish oil an linseed oil containing nanoemulsions) attained using central composite rotable design had desired average hydrodynamic diameter (<130 nm) and narrow PDI along with high percentage transmittance (>95%). The optimized nanoemulsion was transformed into nanoemulsion gel using 1% carbopol-934. The cumulative drug permeated through the skin was 1.3 and 1.4-fold higher for nanoemulsion gel-F and L resp. compared to marketed ointment. The confocal laser scanning microscopy and dermatokinetic studies confirmed enhanced depth of permeation and skin retention (∼1.5-folds) for developed nanoemulsion gel. In vivo study performed on mice using Imiquimod induced psoriasis-like inflammation model, showed significantly high anti-psoriatic activity in mice treated with nanoemulsion gels compared to marketed ointment. Significant reduction in the levels of cytokines (TNF-α and IL-6) in the skin, showed promising outcome in the treatment of psoriasis, of developed nanoemulsion gels compared to marketed ointment. Thus, it was concluded that fish oil and linseed oil integrated tacrolimus nanoemulsion gel could improve the efficacy of tacrolimus and is a promising carrier in the treatment of psoriasis.

Reference of 111-90-0, Diethylene glycol monoethyl ether appears as a colorless, slightly viscous liquid with a mild pleasant odor. Flash point near 190°F. Used to make soaps, dyes, and other chemicals.
Diethylene glycol monoethyl ether is a primary alcohol that is ethanol substituted by a 2-ethoxyethoxy group at position 2. It has a role as a protic solvent. It is a diether, a primary alcohol and a hydroxypolyether. It derives from a diethylene glycol., 111-90-0.

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Ethers lack the hydroxyl groups of alcohols. Without the strongly polarized O―H bond, ether molecules cannot engage in hydrogen bonding with each other. 38256-93-8, formula is C4H11NO, Name is 2-Methoxy-N-methylethanamine. Ethers do have nonbonding electron pairs on their oxygen atoms, however, and they can form hydrogen bonds with other molecules (alcohols, amines, etc.) that have O―H or N―H bonds. COA of Formula: C4H11NO.

Mitsudome, Takato;Noujima, Akifumi;Mizugaki, Tomoo;Jitsukawa, Koichiro;Kaneda, Kiyotomi research published 《 Highly efficient double-carbonylation of amines to oxamides using gold nanoparticle catalysts》, the research content is summarized as follows. Hydrotalcite-supported gold nanoparticles (Au/HT) catalyzed the highly efficient double-carbonylation of amines to oxamides under mild reaction conditions. Various amines were selectively converted to the corresponding oxamides. The cooperation between gold nanoparticles and basic sites of HT plays a key role in the reaction.

COA of Formula: C4H11NO, 2-Methoxy-N-methylethanamine is a useful research compound. Its molecular formula is C4H11NO and its molecular weight is 89.14 g/mol. The purity is usually 95%.
2-Methoxy-N-methylethanamine is a drug that binds to the cannabinoid receptor CB1. It has been shown to be effective in the treatment of cardiac arrhythmia and may also be used as an anti-inflammatory drug. 2MEMEA has been shown to have pharmacokinetic properties that are different from those of other amines, which may be due to its ability to form hydrogen bonds with water molecules. 2MEMEA also has diversified effects on some types of cancer cells, including hyperproliferative and amine-dependent cancers., 38256-93-8.

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Ethers feature bent C–O–C linkages. In dimethyl ether, the bond angle is 111° and C–O distances are 141 pm. 73724-45-5, formula is C18H17NO5, Name is Fmoc-Ser-OH. The barrier to rotation about the C–O bonds is low. The bonding of oxygen in ethers, alcohols, and water is similar. In the language of valence bond theory, the hybridization at oxygen is sp3. Product Details of C18H17NO5.

Mishra, Abhaya Kumar;Tessier, Romain;Hari, Durga Prasad;Waser, Jerome research published 《 Amphiphilic iodine(III) reagents for the lipophilization of peptides in water》, the research content is summarized as follows. We report the functionalization of cysteine residues with lipophilic alkynes bearing a silyl group or an alkyl chain using amphiphilic ethynylbenziodoxolone reagents (EBXs). The reactions were carried out in buffer (pH 6 to 9), without organic co-solvent or removal of oxygen, either at 37°C or room temperature The transformation led to a significant increase of peptide lipophilicity and worked for aromatic thiols, homocysteine, cysteine, and peptides containing 4 to 18 amino acids. His₆-Cys-Ubiquitin was also alkynylated under physiol. conditions. Under acidic conditions, the thioalkynes were converted into thioesters, which could be cleaved in the presence of hydroxylamine.

73724-45-5, Fmoc-Ser-OH, also known as Fmoc-Ser-OH, is a useful research compound. Its molecular formula is C18H17NO5 and its molecular weight is 327.3 g/mol. The purity is usually 95%.
Fmoc-L-Ser-OH is a synthetic peptide that belongs to the group of glycopeptides. It is used as a model for such compounds and has been shown to have antimicrobial activity in vitro against gram-positive bacteria, especially Staphylococcus epidermidis. This compound was synthesized from 3-mercaptopropionic acid and chloride in the presence of hydroxyl groups and epidermal growth factor. The synthetic pathway can be divided into three steps: (1) condensation of 3-mercaptopropionic acid with hydrochloric acid to yield 3-mercaptoacrylic acid; (2) esterification of 3-mercaptoacrylic acid with glycine to form Fmoc-L-Ser; and (3) deprotection of Fmoc protecting group., Product Details of C18H17NO5

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem