30379-58-9

Basic information

• Product Name: BENZYL GLYCOLATE
• Synonyms: BENZYL GLYCOLATE;Benzyl 2-hydroxyacetate;Acetic acid, hydroxy-, phenylMethyl ester;Benzyl glycolate 97%
• CAS NO: 30379-58-9
• Molecular Formula: C₉H₁₀O₃
• Molecular Weight: 166.17
• Product Categories: C8 to C9;Carbonyl Compounds;Esters
• Mol File: 30379-58-9.mol
• Article Data: 33

Chemical Properties

• Boiling Point: 136 °C14 mm Hg(lit.)
• Flash Point: >230 °F
• Appearance: /
• Density: 1.171 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.00296mmHg at 25°C
• Refractive Index: n20/D 1.527(lit.)
• Storage Temp.: Sealed in dry,Room Temperature
• Solubility: Chloroform (Sparingly), Methanol (Slightly)
• PKA: 12.96±0.10(Predicted)
• CAS DataBase Reference: BENZYL GLYCOLATE(CAS DataBase Reference)
• NIST Chemistry Reference: BENZYL GLYCOLATE(30379-58-9)
• EPA Substance Registry System: BENZYL GLYCOLATE(30379-58-9)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 30379-58-9(Hazardous Substances Data)

Usage

Description

BENZYL GLYCOLATE is a benzyl ester of glycolic acid, which is an organic compound with potential applications in various industries due to its unique chemical properties.

Uses

Used in Pharmaceutical Industry:
BENZYL GLYCOLATE is used as a potential moiety for the preparation of phosphonate dipeptides, which serve as potential inhibitors of VanX. This application is significant in the development of new drugs and therapies for various medical conditions.
Used in Chemical Synthesis:
BENZYL GLYCOLATE is used as a key component in the synthesis of various compounds, including methyl [2-(2′-benzyloxy-2′-oxoethyl)-5-acetamido-4,7,8,9-tetra-O-acetyl-3,5-dideoxy-αand -β-D-glycero-D-galacto-2-nonulopyranosid]onate. It is also utilized for the preparation of monosaccharide building blocks, which are essential in the development of new chemical compounds and materials.
Used in Polymer Synthesis:
BENZYL GLYCOLATE is used in the synthesis of new polymeric phosphazenes with pendent esters of glycolic or lactic acid as side units. These polymers include poly[bis(ethyl glycolato)phosphazene], poly[bis(ethyl lactato)phosphazene], poly[bis(benzyl glycolato)phosphazene], and poly[bis(benzyl lactato)phosphazene]. These polymers have potential applications in various industries, such as materials science, pharmaceuticals, and biotechnology, due to their unique properties and potential for customization.

InChI:InChI=1/C9H10O3/c10-6-9(11)12-7-8-4-2-1-3-5-8/h1-5,10H,6-7H2

Upstream product

• 79-14-1 glycolic Acid 
• 100-44-7 benzyl chloride 
• 96-35-5 glycolic acid methyl ester 
• 20194-18-7 sodium phenyl-methanolate 
• 52709-42-9 benzylglyoxylate 
• 100-39-0 benzyl bromide 
• 908094-04-2 phenyldiazomethane 
• 115118-86-0 2-<(tert-butyldimethylsilyl)oxy>acetic acid benzyl ester 
• 100-51-6 benzyl alcohol 

Downstream Products

• 77902-89-7 benzyl <(trifluoromethyl)sulfonyloxy>acetate 
• 152733-51-2 benzyloxycarbonylmethyl O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-acetyl-β-D-glucopyranoside 
• 139116-03-3 Benzyl 2-(Methanesulfonyl)acetate 
• 30379-73-8 benzyl acetoxyacetate 
• 76746-52-6 [[(2R,3S,5R)-2-[Bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yloxy]-(2-cyano-ethoxy)-phosphoryloxy]-acetic acid benzyl ester 
• 135038-13-0 ((2S,5S,6R)-5-Acetoxy-6-acetoxymethyl-5,6-dihydro-2H-pyran-2-yloxy)-acetic acid benzyl ester 
• 135038-15-2 ((2R,5S,6R)-5-Acetoxy-6-acetoxymethyl-5,6-dihydro-2H-pyran-2-yloxy)-acetic acid benzyl ester 
• 74231-20-2 Benzyl<<(trichloroethoxy)carbonyl>oxy>acetate 
• 166043-72-7 Benzyl <<(benzyloxy)<(R,S)-1-<(benzyloxycarbonyl)amino>-2-phenylethyl>phosphoryl>oxy>acetate 
• 183801-52-7 benzyloxycarbonylmethyl 3-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-2-azido-2-deoxy-4,6-O-isopropylidene-α-D-galactopyranoside 
• 183801-57-2 ((2S,3R,4R,5R,6R)-4,5-Diacetoxy-6-acetoxymethyl-3-acetylamino-tetrahydro-pyran-2-yloxy)-acetic acid benzyl ester 
• 1027948-81-7 C₂₄H₃₀N₂O₈S 
• 1027521-68-1 C₁₉H₂₈N₂O₈S 

Relevant articles and documents

Preparation process of methyl glycolate

The preparation process comprises the following steps: firstly adding an organic solvent and glycolic acid into a three-necked flask, stirring at low temperature, adding bromide, and controlling the reaction temperature to be low temperature. The reaction

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