Category: 103-16-2

Micronization of Three Active Pharmaceutical Ingredients Using the Rapid Expansion of Supercritical Solution Technology was written by Fang, Chun-Hao;Chen, Pei-Hua;Chen, Yan-Ping;Tang, Muoi. And the article was included in Chemical Engineering & Technology in 2020.Name: 4-Benzyloxyphenol The following contents are mentioned in the article:

The rapid expansion of supercritical solution (RESS) technol. was applied to recrystallize and micronize three active pharmaceutical ingredients (APIs) of monobenzone, ethylparaben, and kojic acid. All unprocessed (original) APIs had a large mean particle size over 200μm with wide particle size distribution. Supercritical carbon dioxide served as the solvent to extract each API in a high-pressure vessel. The nearly saturated supercritical solution was then expanded through a capillary spray nozzle to ambient pressure state. The APIs were recrystallized in a very short time period. The final API particles with submicron sizes were obtained with much less intensity of crystallinity. The optimal RESS process parameters and the improved result of the in vitro dissolution test for the API of ethylparaben are reported. This study involved multiple reactions and reactants, such as 4-Benzyloxyphenol (cas: 103-16-2Name: 4-Benzyloxyphenol).

4-Benzyloxyphenol (cas: 103-16-2) belongs to ethers. Esters perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Polyesters are important plastics, with monomers linked by ester moieties. Acyl chlorides and acid anhydrides alcoholysis is another way to produce esters. Acyl chlorides and acid anhydrides react with alcohols to produce esters. Anydrous conditions are recommended since both acyl chlorides and acid anhydrides react with water.Name: 4-Benzyloxyphenol

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

Pyridine-based chiral smectogens: effects of polar end groups on liquid crystal properties was written by Vardar, Deniz;Akdas Kilic, Huriye;Ocak, Hale;Jeannin, Olivier;Camerel, Franck;Eran, Belkiz Bilgin. And the article was included in Liquid Crystals in 2021.COA of Formula: C13H12O2 The following contents are mentioned in the article:

In this study, novel chiral pyridine-based rod-like mesogens, consisting of a chloro or bromo group substituted pyridine head core which is connected to one or two aromatic rings through ester linkers and a flexible (S)-2-methylbutoxy or (S)-3,7-dimethyloctyloxy chiral end chain have been synthesized. The liquid crystal properties of new compounds were investigated by various exptl. techniques such as DSC, POM and SAXS. Depending of the nature of the halogen end group, the derivatives with two aromatic rings are non-mesogenic compounds whereas a smectic A phase (SmA) enantiotropically occurs for the members with three aromatic rings of the series. Addnl., chloro group substituted compound composed of three aromatic rings carrying a (S)-2-methylbutoxy end chain exhibits an enantiotropic chiral nematic phase (N*). This study involved multiple reactions and reactants, such as 4-Benzyloxyphenol (cas: 103-16-2COA of Formula: C13H12O2).

4-Benzyloxyphenol (cas: 103-16-2) belongs to ethers. Esters perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Polyesters are important plastics, with monomers linked by ester moieties. Acyl chlorides and acid anhydrides alcoholysis is another way to produce esters. Acyl chlorides and acid anhydrides react with alcohols to produce esters. Anydrous conditions are recommended since both acyl chlorides and acid anhydrides react with water.COA of Formula: C13H12O2

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

Pyridine-based chiral smectogens: effects of polar end groups on liquid crystal properties was written by Vardar, Deniz;Akdas Kilic, Huriye;Ocak, Hale;Jeannin, Olivier;Camerel, Franck;Eran, Belkiz Bilgin. And the article was included in Liquid Crystals in 2021.Formula: C13H12O2 The following contents are mentioned in the article:

In this study, novel chiral pyridine-based rod-like mesogens, consisting of a chloro or bromo group substituted pyridine head core which is connected to one or two aromatic rings through ester linkers and a flexible (S)-2-methylbutoxy or (S)-3,7-dimethyloctyloxy chiral end chain have been synthesized. The liquid crystal properties of new compounds were investigated by various exptl. techniques such as DSC, POM and SAXS. Depending of the nature of the halogen end group, the derivatives with two aromatic rings are non-mesogenic compounds whereas a smectic A phase (SmA) enantiotropically occurs for the members with three aromatic rings of the series. Addnl., chloro group substituted compound composed of three aromatic rings carrying a (S)-2-methylbutoxy end chain exhibits an enantiotropic chiral nematic phase (N*). This study involved multiple reactions and reactants, such as 4-Benzyloxyphenol (cas: 103-16-2Formula: C13H12O2).

4-Benzyloxyphenol (cas: 103-16-2) belongs to ethers. Esters are also usually derived from carboxylic acids. It may also be obtained by reaction of acid anhydride or acid halides with alcohols or by the reaction of salts of carboxylic acids with alkyl halides. Esters are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.Formula: C13H12O2

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

Synthesis, functionalization, and isolation of planar-chiral pillar[5]arenes with bulky substituents using a chiral derivatization agent was written by Al-Azemi, Talal F.;Vinodh, Mickey;Alipour, Fatemeh H.;Mohamod, Abdirahman A.. And the article was included in RSC Advances in 2019.Recommanded Product: 4-Benzyloxyphenol The following contents are mentioned in the article:

Bulky perneopentyloxy-pillar[5]arene (Pillar-1) I was synthesized and its conformational mobility was investigated using variable-temperature ¹H NMR spectroscopy. The host-guest interactions between Pillar-1 I and n-octyltrimethylammonium hexafluorophosphate (OMA) were investigated, and the formation of a 1 : 1 complex was revealed via¹H NMR. Planar-chiral isomers R/S II were synthesized via the reaction of a hydroxy-functionalized pillar[5]arene with chiral derivatization agent (2S)-3,3,3-trifluoro-2-methoxy-2-phenylpropanoyl chloride. The (Sp, R)-and (Rp, R)-forms of the pillar[5]arene diastereomers R/S II were isolated by HPLC, and their structures were analyzed by ¹⁹F NMR. HPLC measurements indicated that racemization did not take place at 40 °C for 72 h. This study involved multiple reactions and reactants, such as 4-Benzyloxyphenol (cas: 103-16-2Recommanded Product: 4-Benzyloxyphenol).

4-Benzyloxyphenol (cas: 103-16-2) belongs to ethers. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits, including apples, durians, pears, bananas, pineapples, and strawberries. Because of their lack of hydrogen-bond-donating ability, esters do not self-associate. Consequently, esters are more volatile than carboxylic acids of similar molecular weight.Recommanded Product: 4-Benzyloxyphenol

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

Synthesis, mesomorphic and dielectric properties of new bent-core liquid crystal with a terminal lactate group was written by Ocak, Hale;Canli, Nimet Yilmaz;Bilgin Eran, Belkiz. And the article was included in Journal of Molecular Structure in 2021.Computed Properties of C13H12O2 The following contents are mentioned in the article:

The synthesis, liquid crystalline properties and dielec. properties of a new bent-core compound (DBOB) composed of terephthalate based rod-like units with a O-dodecyl lactate group substituted at one side as well as n-octyloxy located at other terminal are presented. The liquid crystalline properties have been investigated by polarizing optical microscopy, differential scanning calorimetry and electro-optical studies. The dielec. parameters and phase regions of DBOB, which exhibits an enantiotropic non-polar SmA phase between 156 and 100° as well as SmA phase with a ferroelec. polar response at lower temperatures than 100°, have been carried out by impedance spectroscopy at different temperatures The dielec. relaxation mechanisms have been analyzed by Cole-Cole plots. The Debye distribution parameters and activation energies have also been determined This study involved multiple reactions and reactants, such as 4-Benzyloxyphenol (cas: 103-16-2Computed Properties of C13H12O2).

4-Benzyloxyphenol (cas: 103-16-2) belongs to ethers. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits, including apples, durians, pears, bananas, pineapples, and strawberries. Liquid esters of low volatility serve as softening agents for resins and plastics. Esters also include many industrially important polymers. Polymethyl methacrylate is a glass substitute sold under the names Lucite and Plexiglas; polyethylene terephthalate is used as a film (Mylar) and as textile fibres sold as Terylene, Fortrel, and Dacron.Computed Properties of C13H12O2

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

Synthesis, mesomorphic and dielectric properties of new bent-core liquid crystal with a terminal lactate group was written by Ocak, Hale;Canli, Nimet Yilmaz;Bilgin Eran, Belkiz. And the article was included in Journal of Molecular Structure in 2021.Electric Literature of C13H12O2 The following contents are mentioned in the article:

The synthesis, liquid crystalline properties and dielec. properties of a new bent-core compound (DBOB) composed of terephthalate based rod-like units with a O-dodecyl lactate group substituted at one side as well as n-octyloxy located at other terminal are presented. The liquid crystalline properties have been investigated by polarizing optical microscopy, differential scanning calorimetry and electro-optical studies. The dielec. parameters and phase regions of DBOB, which exhibits an enantiotropic non-polar SmA phase between 156 and 100° as well as SmA phase with a ferroelec. polar response at lower temperatures than 100°, have been carried out by impedance spectroscopy at different temperatures The dielec. relaxation mechanisms have been analyzed by Cole-Cole plots. The Debye distribution parameters and activation energies have also been determined This study involved multiple reactions and reactants, such as 4-Benzyloxyphenol (cas: 103-16-2Electric Literature of C13H12O2).

4-Benzyloxyphenol (cas: 103-16-2) belongs to ethers. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Acyl chlorides and acid anhydrides alcoholysis is another way to produce esters. Acyl chlorides and acid anhydrides react with alcohols to produce esters. Anydrous conditions are recommended since both acyl chlorides and acid anhydrides react with water.Electric Literature of C13H12O2

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

Fluoroalkylation of Various Nucleophiles with Fluoroalkyl Sulfones through a Single Electron Transfer Process was written by Xiao, Pan;Ni, Chuanfa;Miao, Wenjun;Zhou, Min;Hu, Jingyu;Chen, Dingben;Hu, Jinbo. And the article was included in Journal of Organic Chemistry in 2019.Reference of 103-16-2 The following contents are mentioned in the article:

The fluoroalkylation of various nucleophilic reagents with (phenylsulfonyl)difluoromethyl (PhSO₂CF₂)-substituted phenanthridines was achieved to give fluorinated phenanthridine derivatives, which enables the construction of both carbon-heteroatom and carbon-carbon bonds via the substitution of the phenylsulfonyl group. Mechanistic studies indicated that these reactions proceed through a unimol. radical nucleophilic substitution (S_RN1) mechanism. It is worthwhile noting that in the cases of O-nucleophiles (t-BuO^– and PhO^–), the addition of t-BuOK/PhCHO could significantly promote the reactions, due to the in situ formation of a highly reactive electron donor species through the interaction of t-BuOK, PhCHO, and the solvent DMF, which can effectively initiate the single electron transfer process. This study involved multiple reactions and reactants, such as 4-Benzyloxyphenol (cas: 103-16-2Reference of 103-16-2).

4-Benzyloxyphenol (cas: 103-16-2) belongs to ethers. Esters are also usually derived from carboxylic acids. It may also be obtained by reaction of acid anhydride or acid halides with alcohols or by the reaction of salts of carboxylic acids with alkyl halides. Cyclic esters are called lactones, regardless of whether they are derived from an organic or inorganic acid. One example of an organic lactone is γ-valerolactone.Reference of 103-16-2

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

Nanostructured Virus Filtration Membranes Based on Two-Component Columnar Liquid Crystals was written by Hamaguchi, Kazuma;Kuo, Daniel;Liu, Miaomiao;Sakamoto, Takeshi;Yoshio, Masafumi;Katayama, Hiroyuki;Kato, Takashi. And the article was included in ACS Macro Letters in 2019.Formula: C13H12O2 The following contents are mentioned in the article:

Here we report columnar liquid-crystalline (LC) nanostructured membranes that highly remove viruses and show sufficient water permeation. These membranes were prepared by employing two-component liquid crystals that exhibit tetragonal columnar phases. The membranes exhibited virus rejection values of >99.99% (log₁₀ reduction value (LRV) > 4) and water flux ranging from 19 to 61 L m^-2 h^-1 (operation pressure: 0.3 MPa). These membranes were fabricated by photopolymerization of a fan-shaped diol mol. and imidazolium ionic liquid mixture, followed by subsequent removal of the ionic liquid The rejection values and water flux depend on the fraction of ionic liquid These results show new design strategies of materials for the water treatment nanostructured membranes that remove pathogens and contaminants. This study involved multiple reactions and reactants, such as 4-Benzyloxyphenol (cas: 103-16-2Formula: C13H12O2).

4-Benzyloxyphenol (cas: 103-16-2) belongs to ethers. Esters are also usually derived from carboxylic acids. It may also be obtained by reaction of acid anhydride or acid halides with alcohols or by the reaction of salts of carboxylic acids with alkyl halides. Esters are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.Formula: C13H12O2

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

Intramolecular Oxidative Coupling between Unactivated Aliphatic C-H and Aryl C-H Bonds was written by Liao, Yang;Zhou, Yi;Zhang, Zhen;Fan, Junzhen;Liu, Feng;Shi, Zhangjie. And the article was included in Organic Letters in 2021.Name: 4-Benzyloxyphenol The following contents are mentioned in the article:

In this article, a Pd-catalyzed intramol. oxidative coupling between unactivated aliphatic and aryl C-H compounds ROCH₂C(CH₃)₂CO₂H (R = C₆H₅, 4-ClC₆H₄, 2-naphthyl, etc.) has been described. This chem. showed great potential to build up fused cyclic scaffolds I (R¹ = H, Me, OMe; R² = Me, Ph, F, etc.; R³ = H, Me; R⁴ = H, Me; R¹R² = R³R⁴ = -CH=CHCH=CH-) and 3-methyl-3,4-dihydro-2H-benzofuro[2,3-h]chromene-3-carboxylic acid from linear substrates through oxidative couplings. Privileged chromane and tetralin scaffolds were constructed from readily available linear starting materials in the absence of any organohalides and organometallic partners. This study involved multiple reactions and reactants, such as 4-Benzyloxyphenol (cas: 103-16-2Name: 4-Benzyloxyphenol).

4-Benzyloxyphenol (cas: 103-16-2) belongs to ethers. Carboxylic acid esters of low molecular weight are colourless, volatile liquids with pleasant odours, slightly soluble in water. Because of their lack of hydrogen-bond-donating ability, esters do not self-associate. Consequently, esters are more volatile than carboxylic acids of similar molecular weight.Name: 4-Benzyloxyphenol

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

Intramolecular Oxidative Coupling between Unactivated Aliphatic C-H and Aryl C-H Bonds was written by Liao, Yang;Zhou, Yi;Zhang, Zhen;Fan, Junzhen;Liu, Feng;Shi, Zhangjie. And the article was included in Organic Letters in 2021.Reference of 103-16-2 The following contents are mentioned in the article:

In this article, a Pd-catalyzed intramol. oxidative coupling between unactivated aliphatic and aryl C-H compounds ROCH₂C(CH₃)₂CO₂H (R = C₆H₅, 4-ClC₆H₄, 2-naphthyl, etc.) has been described. This chem. showed great potential to build up fused cyclic scaffolds I (R¹ = H, Me, OMe; R² = Me, Ph, F, etc.; R³ = H, Me; R⁴ = H, Me; R¹R² = R³R⁴ = -CH=CHCH=CH-) and 3-methyl-3,4-dihydro-2H-benzofuro[2,3-h]chromene-3-carboxylic acid from linear substrates through oxidative couplings. Privileged chromane and tetralin scaffolds were constructed from readily available linear starting materials in the absence of any organohalides and organometallic partners. This study involved multiple reactions and reactants, such as 4-Benzyloxyphenol (cas: 103-16-2Reference of 103-16-2).

4-Benzyloxyphenol (cas: 103-16-2) belongs to ethers. Carboxylic acid esters of low molecular weight are colourless, volatile liquids with pleasant odours, slightly soluble in water. Esters are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.Reference of 103-16-2

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