All Photos(1)
Select a Size
Change View
5 ML
$90.06
25 ML
$332.50
About This Item
Linear Formula:
HOCH2CO2CH2C6H5
CAS Number:
Molecular Weight:
166.17
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
assay
97%
form
liquid
refractive index
n20/D 1.527 (lit.)
bp
136 °C/14 mmHg (lit.)
density
1.171 g/mL at 25 °C (lit.)
functional group
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
Looking for similar products? Visit Product Comparison Guide
General description
Benzyl glycolate is a benzyl ester of glycolic acid.
Application
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.[1] It may be used for the preparation of monosaccharide building blocks.[2] 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:[3]
- poly[bis(ethyl glycolato)phosphazene]
- poly[bis(ethyl lactato)phosphazene]
- poly[bis(benzyl glycolato)phosphazene]
- poly[bis(benzyl lactato)phosphazene]
Storage Class
10 - Combustible liquids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Chien-Tai Ren et al.
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
Chien-Tai Ren et al.
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.
Allcock HR, et al.
Macromolecules, 27(1), 1-4 (1994)
Active Filters
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service
