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Benzyl glycinate hydrochloride

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Benzyl glycinate hydrochloride Basic information

Product Name:
Benzyl glycinate hydrochloride
Synonyms:
  • Gly-OBzl·HCl
  • L-A-AMINOPHENYLACETIC ACID METHYL ESTER HYDROCHLORI
  • H-Gly-OBzl.HCl,Benzylglycinate
  • benzyl glycinate
  • GLYCINE BENZYL ESTERHCI
  • Glycinebenzylester·HCl,Glycinebenzylesterhydrochloride
  • BENZYL GLYCINATE HYDROCHLORIDE
  • L-GLYCINE BENZYL ESTER HYDROCHLORIDE
CAS:
2462-31-9
MF:
C9H12ClNO2
MW:
201.65
Product Categories:
  • Amino Acids & Derivatives
  • Inhibitors
  • Glycine [Gly, G]
  • Amino hydrochloride
  • Amino Acid Derivatives
Mol File:
2462-31-9.mol
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Benzyl glycinate hydrochloride Chemical Properties

Melting point:
138-140°C
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
solubility 
DMSO, Methanol, Water
form 
Solid
color 
White to Off-White
InChI
InChI=1S/C9H11NO2.ClH/c10-6-9(11)12-7-8-4-2-1-3-5-8;/h1-5H,6-7,10H2;1H
InChIKey
VLQHNAMRWPQWNK-UHFFFAOYSA-N
SMILES
C1(=CC=CC=C1)COC(=O)CN.Cl
CAS DataBase Reference
2462-31-9(CAS DataBase Reference)
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Safety Information

Safety Statements 
22-24/25
WGK Germany 
3
HS Code 
29224999
Storage Class
11 - Combustible Solids

MSDS

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Benzyl glycinate hydrochloride Usage And Synthesis

Chemical Properties

White Solid

Uses

Potent crosslinking inhibitors.

Biological Activity

The benzyl ester group of the amino acid monomers promote kinetically controlled synthesis (KCS) of polypeptides by increasing the substrate affinity and specificity of the enzyme. It is useful in the chemoenzymatic polymerization of glycine monomers.

Synthesis

N-Boc glycine (2.85 mmol), benzyl alcohol (2.85 mmol), 1-ethyl-(3-dimethylaminopropyl)carbodiimide hydrochloride (3.71 mmol) and DMAP (0.6 mmol) were reacted in dichloromethane at 25 ??C with stirring overnight. At the end of the reaction the reaction mixture was extracted with ethyl acetate and the resulting organic layer was washed with brine. The organic layer was separated and dried over anhydrous Na2SO4, the desiccant was removed by filtration and the resulting filtrate was concentrated under vacuum to evaporate the organic solvent. The resulting residue was purified by silica gel column chromatography (PE: EA = 2:1) to afford the compound with the amino group protected by Boc. Finally, a solution of dilute hydrochloric acid in ethyl acetate was added to the crude product and the resulting reaction mixture was reacted at 0 degree C for 2-3 hours to afford the target product molecule glycine benzyl ester hydrochloride.

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