추천 제품
Quality Level
분석
97%
형태
liquid
refractive index
n20/D 1.527 (lit.)
bp
136 °C/14 mmHg (lit.)
density
1.171 g/mL at 25 °C (lit.)
작용기
ester
hydroxyl
phenyl
SMILES string
OCC(=O)OCc1ccccc1
InChI
1S/C9H10O3/c10-6-9(11)12-7-8-4-2-1-3-5-8/h1-5,10H,6-7H2
InChI key
VPYJBEIOKFRWQZ-UHFFFAOYSA-N
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일반 설명
Benzyl glycolate is a benzyl ester of glycolic acid.
애플리케이션
Benzyl glycolate may be used for the synthesis of the methyl [2-(2′-benzyloxy-2′-oxoethyl)-5-acetamido-4,7,8,9- tetra-O-acetyl-3,5-dideoxy-α- and -β-D-glycero-D-galacto-2-nonulopyranosid]onate. It may be used for the preparation of monosaccharide building blocks. It may also be used for the synthesis of the following new polymeric phosphazenes having pendent esters of glycolic or lactic acid as side units:
- poly[bis(ethyl glycolato)phosphazene]
- poly[bis(ethyl lactato)phosphazene]
- poly[bis(benzyl glycolato)phosphazene]
- poly[bis(benzyl lactato)phosphazene]
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Gloves
Chemistry (Weinheim an der Bergstrasse, Germany), 9(5), 1085-1095 (2003-02-22)
A facile synthesis of the sialic acid oligomers alpha-(2-->5)Neu5Gc (1) is presented. Monosaccharides 2-4 with suitable functionality were used as the building blocks. After selective removal of the paired carboxyl and amine protecting groups, the fully protected oligomers were assembled
The Journal of organic chemistry, 67(4), 1376-1379 (2002-02-16)
The preparation of a disaccharide 2, Neu5Ac-alpha-(2-->5)Neu5Gc having a alpha-benzyl protecting group at the reducing end, by the coupling of the easily accessible building units 4 and 5 is described. Subsequent deprotection of the coupling adduct led to the isolation
Synthesis of poly (orgnaophosphazenes) with glycolic acid ester and lactic acid ester side groups: Prototypes for new bioerodible polymers.
Macromolecules, 27(1), 1-4 (1994)
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