BENZYL GLYCOLATE

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Names

[ CAS No. ]:
30379-58-9

[ Name ]:
BENZYL GLYCOLATE

[Synonym ]:
O-benzylglycolic acid
Acetic acid,hydroxy-,phenylmethyl ester
glycolic acid benzyl ester
2-hydroxybenzyl acetate
Benzyl (1)-glycolate
Benzyl glycolate
Benzyl hydroxyacetate
MFCD00191776

Chemical & Physical Properties

[ Density]:
1.171 g/mL at 25ºC(lit.)

[ Boiling Point ]:
136ºC14 mm Hg(lit.)

[ Molecular Formula ]:
C9H10O3

[ Molecular Weight ]:
166.17400

[ Flash Point ]:
>230 °F

[ Exact Mass ]:
166.06300

[ PSA ]:
46.53000

[ LogP ]:
0.72210

[ Index of Refraction ]:
n20/D 1.527(lit.)

[ Storage condition ]:
2-8°C

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves

[ Hazard Codes ]:
Xi

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2918199090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • Glycolic acid
  • Benzyl bromide
  • Benzyl alcohol
  • BENZYLGLYOXYLATE; >97DISCONTINUED 04/04/01
  • Benzyl chloride
  • benzyl 2-[tert-butyl(dimethyl)silyl]oxyacetate
  • Methyl glycolate
  • SODIUM BENZYLOXIDE

DownStream

  • benzyl 2-prop-2-enoxyacetate
  • benzyl 2-[tert-butyl(dimethyl)silyl]oxyacetate
  • Glycolic acid
  • ethyl 2-trityloxyacetate

Customs

[ HS Code ]: 2918199090

[ Summary ]:
2918199090 other carboxylic acids with alcohol function but without other oxygen function, their anhydrides, halides, peroxides, peroxyacids and their derivatives。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:6.5%。General tariff:30.0%

Articles

Synthesis of a sialic acid dimer derivative, 2'alpha-O-benzyl Neu5Ac-alph-(2-->5)Neu5Gc.

J. Org. Chem. 67(4) , 1376-79, (2002)

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...

Synthesis of alpha-(2-->5)Neu5Gc oligomers.

Chemistry 9(5) , 1085-95, (2003)

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 p...

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)


More Articles

Related Compounds

  • benzyl 3-diaziridin-1-ylphosphoryloxypropanoate
  • benzyl 1-(2-naphthyl)ethyl sulfide
  • Benzyl 3-isothiocyanatophenyl ether
  • benzyl N-[1-phenyl-5-(pyrrol-1-yl)-1H-pyrazol-4-yl]carbamate
  • Benzyl (2R,3S,5S)-3-(benzyloxy)-2-hexyl-5-hydroxyhexadecanoate
  • Benzyl 5-Fluoropiperidin-3-Ylcarbamate Hydrochloride
  • 6-Bromo-4-fluoro-1-isopropyl-2-(methoxymethyl)-1H-benzo[d]imidazole
  • 6-bromo-4-fluoro-1-isopropyl-1,3-dihydro-2H-benzo[d]imidazole-2-one
  • 6-Bromo-2-(difluoromethyl)-4-fluoro-1-propan-2-ylbenzimidazole
  • 6-Bromo-4-(tert-butoxy)-1-isopropyl-2-methyl-1H-benzo[d]imidazole
  • 1,3-Dimethyl-5-[3-(2-piperidinyl)phenyl]-2(1h)-pyridinone
  • 1,7-Dimethyl-1H-pyrazolo[3,4-c]pyridine
  • 3-[(3-Cyclopropyl-1,2,4-oxadiazol-5-yl)methyl]piperidin-3-ol
  • 6-Chloro-2-methylbenzo[b]thiophen-3-ol
  • 1-(Boc-amino)-5-(2-hydroxyethoxy)pentane
  • 2-(1-Aminopropan-2-yl)bicyclo[4.1.0]heptan-2-ol
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