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Benzyloxyacetic acid

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Benzyloxyacetic acid Basic information

Product Name:
Benzyloxyacetic acid
Synonyms:
  • PHENYLMETHOXY ACETIC ACID
  • RARECHEM AL BE 0628
  • BENZYLOXYACETIC ACID
  • ACETIC ACID, (PHENYLMETHOXY)-
  • benzyloxy acctic acid
  • 2-(benzyloxy)acetic acid
  • Acetic acid, 2-(phenylMethoxy)-
  • Benzyloxyacetic acid 95%
CAS:
30379-55-6
MF:
C9H10O3
MW:
166.17
Product Categories:
  • Building Blocks/Intermediates
  • C9
  • Carbonyl Compounds
  • Carboxylic Acids
Mol File:
30379-55-6.mol
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Benzyloxyacetic acid Chemical Properties

Melting point:
80-81 °C
Boiling point:
137-139 °C/0.6 mmHg (lit.)
Density 
1.162 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.526(lit.)
Flash point:
>230 °F
storage temp. 
Sealed in dry,Room Temperature
form 
clear liquid
pka
3.52±0.10(Predicted)
color 
Colorless to Light orange to Yellow
CAS DataBase Reference
30379-55-6(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29189900

MSDS

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Benzyloxyacetic acid Usage And Synthesis

Chemical Properties

Colorless liquid

Uses

It is a compound for proteomics research use. It may be used for following synthesis mixed benzyloxyacetic pivalic anhydride, chiral glycolates, 1,2:4,5-di-O-isopropylidene-β-D-fructopyranos-3-yl benzyloxyacetate, via esterification, tetra aqua(1,10-phenanthroline-[κ]2N,N?)magnesium(II) bis[(2,4-dichlorophenyl)acetate], as ligand in the preparation of diaquabis(benzyloxyacetato)copper(II) complex.

Uses

Benzyloxyacetic acid may be used for the following syntheses:

  • mixed benzyloxyacetic pivalic anhydride
  • chiral glycolates, 1,2:4,5-di-O-isopropylidene-β-D-fructopyranos-3-yl benzyloxyacetate, via esterification
  • tetraaqua(1,10-phenanthroline-[κ]2N,N′)magnesium(II) bis[(2,4-dichlorophenyl)acetate]
  • as ligand in the preparation of diaquabis(benzyloxyacetato)copper(II) complex

Definition

ChEBI: (benzyloxy)acetic acid is a monocarboxylic acid that is benzyl alcohol in which the hydroxy group is replaced by a carboxymethoxy group. It is a monocarboxylic acid, an ether and a member of benzenes. It is functionally related to a benzyl alcohol and a glycolic acid.

General Description

In vitro activities of phenoxy and benzyloxyacetic acid derivatives as antisickling agents has been investigated by the application of quantitative structure activity relationship (QSAR) of Hansch-type.

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