Dickschat, Jeroen S’s team published research in Beilstein Journal of Organic Chemistry in 2018 | 56724-03-9

Beilstein Journal of Organic Chemistry published new progress about Aromatic compounds Role: BSU (Biological Study, Unclassified), BIOL (Biological Study). 56724-03-9 belongs to class ethers-buliding-blocks, and the molecular formula is C9H10O2, Electric Literature of 56724-03-9.

Dickschat, Jeroen S.; Wang, Tao; Stadler, Marc published the artcile< Volatiles from the xylarialean fungus Hypoxylon invadens>, Electric Literature of 56724-03-9, the main research area is Hypoxylon fungal volatile natural product constitutional isomer; constitutional isomerism; gas chromatography; mass spectrometry; natural products; volatiles.

The volatiles emitted by agar plate cultures of the xylarialean fungus Hypoxylon invadens were investigated by use of a closed loop stripping apparatus in combination with GC-MS. Several aromatic compounds were found that could only be identified by comparison to all possible constitutional isomers with different ring substitution patterns. For the set of identified compounds a plausible biosynthetic scheme was suggested that gives further support for the assigned structures.

Beilstein Journal of Organic Chemistry published new progress about Aromatic compounds Role: BSU (Biological Study, Unclassified), BIOL (Biological Study). 56724-03-9 belongs to class ethers-buliding-blocks, and the molecular formula is C9H10O2, Electric Literature of 56724-03-9.

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

Harwood, Laurence M’s team published research in Tetrahedron Letters in 1987 | 52244-70-9

Tetrahedron Letters published new progress about Cyclic ethers Role: SPN (Synthetic Preparation), PREP (Preparation). 52244-70-9 belongs to class ethers-buliding-blocks, and the molecular formula is C11H16O2, Application In Synthesis of 52244-70-9.

Harwood, Laurence M.; Robertson, Jeremy published the artcile< Preparation of cyclic ethers via oxidative cyclization of 2-(4-hydroxyalkyl)- and 2-(5-hydroxyalkyl)furans with DDQ>, Application In Synthesis of 52244-70-9, the main research area is hydroxyalkylfuran oxidative cyclization; ether cyclic; furyltetrahydrofuran.

Reaction of hydroxyalkylfurans I [n = 2, R = H, R1 = H, C(:CH2)COMe, 5-methyl-2-furyl; n = 2, RR1 = O; n = 3, R = H, R1 = 5-methyl-2-furyl] with DDQ gave cyclic ethers II under neutral conditions. Aromatic analogs do not give useful yields of desired products.

Tetrahedron Letters published new progress about Cyclic ethers Role: SPN (Synthetic Preparation), PREP (Preparation). 52244-70-9 belongs to class ethers-buliding-blocks, and the molecular formula is C11H16O2, Application In Synthesis of 52244-70-9.

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

Huang, Shuang’s team published research in Dalton Transactions in 2019 | 10541-78-3

Dalton Transactions published new progress about Benzoxazoles Role: CAT (Catalyst Use), PRP (Properties), RCT (Reactant), SPN (Synthetic Preparation), USES (Uses), RACT (Reactant or Reagent), PREP (Preparation). 10541-78-3 belongs to class ethers-buliding-blocks, and the molecular formula is C8H11NO, Related Products of 10541-78-3.

Huang, Shuang; Hong, Xi; Cui, He-Zhen; Zhou, Quan; Lin, Yue-Jian; Hou, Xiu-Feng published the artcile< N-Methylation of ortho-substituted aromatic amines with methanol catalyzed by 2-arylbenzo[d]oxazole NHC-Ir(III) complexes>, Related Products of 10541-78-3, the main research area is arylamine methanol arylbenzoxazole iridium complex catalyst methylation green chem; methyl arylamine preparation.

Seven new chelated cyclometalated Ir complexes of ABON,P, ABON,O and ABON,C(carbene) based on a rigid and tunable 2-arylbenzo[d]oxazole backbone were prepared for the N-methylation of amines. Among these three coordinated modes, ABON,C(carbene)-chelated iridium-based catalysts exhibited good performance in the monomethylation of aromatic amines with methanol (MeOH) as the green methylation reagent. The steric-modified synthesis of ABON,C(carbene) complexes was described. The most active ABON,C(carbene) complex with marginal steric hindrance as a catalyst was obtained from the benzoxazole ring without a substituent and Me group of the benzimidazole ring on the N-heterocyclic carbene (NHC) ligand. A variety of amines including para- and meta-substituted aromatic amines, as well as heterocyclic amines, were formulated as suitable substrates. Importantly, this catalyst considerably promoted the yield of the N-methylation of ortho-substituted aromatic amines. Controlled kinetic experiments and deuterium-labeling reactions of these ortho-substituted amines were conducted under optimized conditions. On the basis of the exptl. results, a plausible mechanism was proposed.

Dalton Transactions published new progress about Benzoxazoles Role: CAT (Catalyst Use), PRP (Properties), RCT (Reactant), SPN (Synthetic Preparation), USES (Uses), RACT (Reactant or Reagent), PREP (Preparation). 10541-78-3 belongs to class ethers-buliding-blocks, and the molecular formula is C8H11NO, Related Products of 10541-78-3.

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

Qi, Li’s team published research in Journal of Pharmaceutical Sciences (Philadelphia, PA, United States) in 2021-11-30 | 18312-57-7

Journal of Pharmaceutical Sciences (Philadelphia, PA, United States) published new progress about Bioavailability. 18312-57-7 belongs to class ethers-buliding-blocks, and the molecular formula is C17H37NO2, Recommanded Product: 2,2′-(Tridecylazanediyl)diethanol.

Qi, Li; Liu, Jian; Ronk, Michael; Gallegos, Alejandra; Fujimori, Kiyoshi; Luo, Yanxin; Li, Kim; Lee, Hans; Nashed-Samuel, Yasser published the artcile< A Holistic Approach of Extractables and Leachables Assessment of Rubber Stoppered Glass Vial Systems for Biotechnology Products>, Recommanded Product: 2,2′-(Tridecylazanediyl)diethanol, the main research area is rubber stoppered glass vial extractable leachable biotechnol; Extractables; Glass vials; Holistic approach; ICH Q3D; Leachables; Rubber stoppers; Toxicology.

Rubber stoppered glass vial systems are widely used as primary containers for storing and delivering therapeutic protein products to patients. Addressing concerns and regulatory expectations related to the risk to biol. drug product quality and patient safety from rubber stoppered glass vial systems requires implementation of an extractable and leachable evaluation program based on material understanding, risk assessment, literature review, and a comprehensive scientifically sound anal. testing methodol. The extractable and leachable study design consisted of twelve drug products filled in twelve different size glass vials capped with laminated and nonlaminated rubber stoppers made from three different rubber formulations. Design of the model solvents was successful as they had little to no anal. interference and mimicked the formulation conditions and generated representative extractables capable of predicting leachables. The extraction conditions of time and temperature were appropriate as not to degrade the test materials or the extractable compounds, and yet generated significant quantities for identification of the extractable compounds with confidence. The extractables testing results were capable of predicting the leachable profiles of the twelve drug products. In each case, the leachable profile was a subset of the extractable profile. The organic and elemental impurities of the leachable profiles of drug products were the end-to-end verification of the quality of the glass vials, rubber stoppers and drug product lifecycles. Overall, the holistic approach was fully successful in the qualification of different vial systems as primary containers and delivery systems for different biotherapeutic products to ensure product quality and patient safety.

Journal of Pharmaceutical Sciences (Philadelphia, PA, United States) published new progress about Bioavailability. 18312-57-7 belongs to class ethers-buliding-blocks, and the molecular formula is C17H37NO2, Recommanded Product: 2,2′-(Tridecylazanediyl)diethanol.

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

Urakawa, Kazuki’s team published research in Organic Letters in 2018-05-04 | 56724-03-9

Organic Letters published new progress about Antiaromaticity (of keto carbenium ion). 56724-03-9 belongs to class ethers-buliding-blocks, and the molecular formula is C9H10O2, Computed Properties of 56724-03-9.

Urakawa, Kazuki; Kawabata, Yuta; Matsuda, Masaki; Sumimoto, Michinori; Ishikawa, Hayato published the artcile< α-Ketocarbenium Ions Derived from Orthoquinone-Containing Polycyclic Aromatic Compounds>, Computed Properties of 56724-03-9, the main research area is keto carbenium ion preparation orthoquinone PAH absorption spectra.

α-Ketocarbenium ions derived from synthesized orthoquinone-containing polycyclic aromatic compounds were generated in the presence of Bronsted acids such as sulfuric acid, trifluoromethanesulfonic acid, and fluorosulfonic acid. The prepared α-ketocarbenium ions were stabilized by conjugation of the aromatic moiety. In addition, unique absorption properties of the α-ketocarbenium ions were observed and identified on the basis of the calculated absorption spectra. It was suggested that the zigzag-shaped architecture stabilizes the newly discovered α-ketocarbenium ions derived from orthoquinone-containing polycyclic aromatic compounds

Organic Letters published new progress about Antiaromaticity (of keto carbenium ion). 56724-03-9 belongs to class ethers-buliding-blocks, and the molecular formula is C9H10O2, Computed Properties of 56724-03-9.

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

Oestreich, M’s team published research in Science of Synthesis in 2007 | 56724-03-9

Science of Synthesis published new progress about Aryl aldehydes Role: SPN (Synthetic Preparation), PREP (Preparation). 56724-03-9 belongs to class ethers-buliding-blocks, and the molecular formula is C9H10O2, Computed Properties of 56724-03-9.

Oestreich, M. published the artcile< Arenecarbaldehydes: synthesis by C-C bond formation>, Computed Properties of 56724-03-9, the main research area is review arenecarbaldehyde preparation bond formation organic synthesis.

A review of methods to prepare arenecarbaldehydes by C-C bond formation.

Science of Synthesis published new progress about Aryl aldehydes Role: SPN (Synthetic Preparation), PREP (Preparation). 56724-03-9 belongs to class ethers-buliding-blocks, and the molecular formula is C9H10O2, Computed Properties of 56724-03-9.

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

Akagi, Yusuke’s team published research in Chemical & Pharmaceutical Bulletin in 2020 | CAS: 529-28-2

1-Iodo-2-methoxybenzene(cas: 529-28-2) participates in palladium catalyzed enantioselective Heck arylation of 2,3-dihydrofuran in the presence of chiral ionic liquids containing L-prolinate and L-lactate anions and non-chiral quaternary ammonium cations.Electric Literature of C7H7IO

《Palladium-catalyzed β-arylation of cyclic α,β,-unsaturated O-methyl oximes with aryl iodides》 was published in Chemical & Pharmaceutical Bulletin in 2020. These research results belong to Akagi, Yusuke; Fukuyama, Shiori; Komatsu, Toshiya. Electric Literature of C7H7IO The article mentions the following:

A Pd-catalyzed β-arylation of cyclic α,β-unsaturated O-Me oximes with substituted iodobenzenes was reported. This reaction showed complete regioselectivity and excellent functional group tolerance. The β-arylation of 2-cyclohexen-1-one O-Me oxime (existing as 2:1 E/Z mixture) with certain aryl iodides such as 4-iodoanisole afforded only β-arylated (E)-O-Me oximes. The results came from multiple reactions, including the reaction of 1-Iodo-2-methoxybenzene(cas: 529-28-2Electric Literature of C7H7IO)

1-Iodo-2-methoxybenzene(cas: 529-28-2) participates in palladium catalyzed enantioselective Heck arylation of 2,3-dihydrofuran in the presence of chiral ionic liquids containing L-prolinate and L-lactate anions and non-chiral quaternary ammonium cations.Electric Literature of C7H7IO

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

Kerru, Nagaraju’s team published research in Applied Organometallic Chemistry in 2020 | CAS: 135-02-4

2-Methoxybenzaldehyde(cas: 135-02-4) is used as a flavor agent in foods including nonalcoholic/alcoholic beverages, baked goods, chewing gum, confections, frozen dairy, fruit ices, hard/soft candy, instant coffee, tea, Jams, jellies, and milk products. It also has been used to obtain good enantioselectivities using Cu(OAc)(2)-bis(oxazolines) via hydrogen bonding in asymmetric Henry reaction.HPLC of Formula: 135-02-4

《Bi2O3/FAp, a sustainable catalyst for synthesis of dihydro-[1,2,4]triazolo[1,5-a]pyrimidine derivatives through green strategy》 was published in Applied Organometallic Chemistry in 2020. These research results belong to Kerru, Nagaraju; Gummidi, Lalitha; Maddila, Surya Narayana; Bhaskaruni, Sandeep V. H. S.; Jonnalagadda, Sreekantha B.. HPLC of Formula: 135-02-4 The article mentions the following:

The bismuth loaded on fluorapatite (Bi2O3/FAp) proved to be an excellent catalyst for the synthesis of novel dihydro-[1,2,4]triazolo[1,5-a]pyrimidine derivatives I (R = 4-methoxyphenyl, 2-nitrophenyl, indol-3-yl, etc.; R1 = Me, NH2) via a three-component reaction involving the mixture of 1H-1,2,4-triazol-5-amine, Et cyanoacetate or Et acetoacetate, and different benzaldehydes RCHO in ethanol at room temperature The catalyst material was characterized by X-ray diffraction, Brunauer-Emmett-Teller surface area anal., Fourier-transform IR, SEM, energy-dispersive X-ray spectroscopy, and transmission electron microscopy techniques. The efficacy of Bi2O3/FAp as a heterogeneous catalyst was evaluated with the loading of different weight% of bismuth on FAp. The 2.5% bismuth on FAp performed extremely well as a catalyst with a high yield of products (92%-96%) in a short reaction time (25-35 min). The catalyst was recovered by simple filtration. It showed undiminished activity up to five runs. Simple work-up, room temperature reaction, short reaction time, high yields, no column chromatog., and good reusability of catalyst are the merits of the proposed protocol. In addition, this process offers 100% carbon efficiency and 98% atom economy with noteworthy fiscal and environmental benefits. In the experimental materials used by the author, we found 2-Methoxybenzaldehyde(cas: 135-02-4HPLC of Formula: 135-02-4)

2-Methoxybenzaldehyde(cas: 135-02-4) is used as a flavor agent in foods including nonalcoholic/alcoholic beverages, baked goods, chewing gum, confections, frozen dairy, fruit ices, hard/soft candy, instant coffee, tea, Jams, jellies, and milk products. It also has been used to obtain good enantioselectivities using Cu(OAc)(2)-bis(oxazolines) via hydrogen bonding in asymmetric Henry reaction.HPLC of Formula: 135-02-4

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

Chavan, Pravin’s team published research in Journal of Heterocyclic Chemistry in 2020 | CAS: 673-22-3

2-Hydroxy-4-methoxybenzaldehyde(cas: 673-22-3) is employed in the synthesis of Schiff base ligand. It is applied as a reactant in the synthesis of LPA1R antagonists used in the inhibition of LPA-induced proliferation and contraction of normal human lung fibroblasts. Also used in the synthesis of tyrosine kinase 6 proteinase inhibitors.Product Details of 673-22-3

《Synthesis of substituted pyrimidine using ZnFe2O4 nanocatalyst via one pot multi-component reaction ultrasonic irradiation》 was published in Journal of Heterocyclic Chemistry in 2020. These research results belong to Chavan, Pravin; Bangale, Sachin; Pansare, Dattatraya; Shelke, Rohini; Jadhav, Shivaji; Tupare, Shrikrushna; Kamble, Dhanraj; Rai, Megha. Product Details of 673-22-3 The article mentions the following:

A highly efficient, eco-friendly, recyclable heterogeneous ZnFe2O4 nanocatalyzed synthesis of 2-amino-4-substituted 1,4-dihydrobenzo[4,5]imidazo[1,2-a]pyrimidine-3-carbonitrile derivatives I (R = 4-chlorophenyl, 4-hydroxyphenyl, 2,4-dichlorophenyl, 3-bromophenyl, etc.) via one pot multicomponent reaction of 1H-1,3-benzodiazol-2-amine, substituted aromatic aldehyde RCHO and malononitrile under ultrasonic irradiations is described. Significance of this synthetic approach is short reaction time, easy handling, simplicity, efficiency, high yield, and recoverable catalyst. The experimental part of the paper was very detailed, including the reaction process of 2-Hydroxy-4-methoxybenzaldehyde(cas: 673-22-3Product Details of 673-22-3)

2-Hydroxy-4-methoxybenzaldehyde(cas: 673-22-3) is employed in the synthesis of Schiff base ligand. It is applied as a reactant in the synthesis of LPA1R antagonists used in the inhibition of LPA-induced proliferation and contraction of normal human lung fibroblasts. Also used in the synthesis of tyrosine kinase 6 proteinase inhibitors.Product Details of 673-22-3

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

Martzel, Thomas’s team published research in Chemistry – A European Journal in 2020 | CAS: 60656-87-3

2-(Benzyloxy)acetaldehyde(cas: 60656-87-3) may be used in the following syntheses: (3S,5S)-methyl 6-benzyloxy-3,5-dihydroxyhexanoate ,(S)-5-benzyloxy-4-hydroxypentan-2-one, myxothiazols.SDS of cas: 60656-87-3

《Organocatalytic multicomponent synthesis of α/β-dipeptide derivatives》 was published in Chemistry – A European Journal in 2020. These research results belong to Martzel, Thomas; Annibaletto, Julien; Millet, Pierre; Pair, Etienne; Sanselme, Morgane; Oudeyer, Sylvain; Levacher, Vincent; Briere, Jean-Francois. SDS of cas: 60656-87-3 The article mentions the following:

A straightforward multicomponent Knoevenagel-aza-Michael-cyclocondensation reaction involving readily available hydroxamic acid-derived from naturally occurring α-amino acids allows a diversity-oriented synthesis of novel isoxazolidin-5-ones possessing an N-protected α-amino acid pendant with good to high diastereoselectivities thanks to a match effect with a chiral organocatalyst. These diversely substituted heterocycles, easily isolated as a single diastereoisomer, proved to be versatile platforms for the formation of an array of α/β-dipeptide fragments. The experimental part of the paper was very detailed, including the reaction process of 2-(Benzyloxy)acetaldehyde(cas: 60656-87-3SDS of cas: 60656-87-3)

2-(Benzyloxy)acetaldehyde(cas: 60656-87-3) may be used in the following syntheses: (3S,5S)-methyl 6-benzyloxy-3,5-dihydroxyhexanoate ,(S)-5-benzyloxy-4-hydroxypentan-2-one, myxothiazols.SDS of cas: 60656-87-3

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