H-Gly-OBZl.HCl

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Names

[ CAS No. ]:
2462-31-9

[ Name ]:
H-Gly-OBZl.HCl

[Synonym ]:
GLYCINE-OBZL HCL
GLYCINE BENZYL ESTER HCL
Benzyl glycinate HCl
Benzyl glycinate hydrochloride (1:1)
Benzyl glycinate hyd
N-Bn-glycine hydrochloride
GLYCINE BENZYL ESTERHCI
MFCD00035442
GLY-OBZLCL
Glycine, phenylmethyl ester, hydrochloride (1:1)
Glycine, N-(phenylmethyl)-, hydrochloride (1:1)
Benzyl glycinate
Gly benzyl ester hydrochloride
H2N-Gly-OBn*HCl
H-Gly-OBZl,HCl
benzyl 2-aminoacetate hydrochloride
Glycine benzyl ester hydrochloride
GlyOBn hydrochloride
Benzyl Glycinate Hydrochloride
H-Gly-OBzl.HCl,Benzylglycinate
Benzylglycinatehydrochloride
H-Gly-Obzl.HCl
N-Benzylglycine hydrochloride (1:1)
H-Gly-OBzl·HCl

Chemical & Physical Properties

[ Density]:
1.132g/cm3

[ Boiling Point ]:
245.5ºC at 760 mmHg

[ Melting Point ]:
138-140°C

[ Molecular Formula ]:
C9H12ClNO2

[ Molecular Weight ]:
201.650

[ Flash Point ]:
110.3ºC

[ Exact Mass ]:
201.055649

[ PSA ]:
52.32000

[ LogP ]:
2.19080

[ Vapour Pressure ]:
0.0146mmHg at 25°C

[ Index of Refraction ]:
1.558

[ Storage condition ]:
−20°C

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xi

[ Safety Phrases ]:
S22-S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • Glycine
  • Benzyl alcohol
  • Benzyl 2-[(2-methylpropan-2-yl)oxycarbonylamino]acetate

DownStream

  • BENZYL2-AMINOACETATEHYDROCHLORIDE
  • benzyl 2-[(2-phenylmethoxycarbonylaminoacetyl)amino]acetate
  • Glycine,N-(N-carboxy-DL-seryl)-, dibenzyl ester (6CI,8CI)
  • Benzyl N-(diphenylmethylene)glycinate
  • Glycine,N-[N-[(phenylmethoxy)carbonyl]-S-(phenylmethyl)-L-cysteinyl]-, phenylmethylester (9CI)
  • benzyl 2-[2-(phenylmethoxycarbonylamino)propanoylamino]acetate
  • 1H-indole-2-carboxylic acid benzyl ester
  • benzyl 2-isocyanoacetate
  • benzyl N-benzyloxycarbonylglycinate

Articles

The Benzyl Ester Group of Amino Acid Monomers Enhances Substrate Affinity and Broadens the Substrate Specificity of the Enzyme Catalyst in Chemoenzymatic Copolymerization.

Biomacromolecules 17 , 314-23, (2016)

The chemoenzymatic polymerization of amino acid monomers by proteases involves a two-step reaction: the formation of a covalent acyl-intermediate complex between the protease and the carboxyl ester gr...

Synthesis of a metabolite of metoclopramide and its detection in human urine.

Il Farmaco 49 , 805-808, (1994)

The synthesis of 2-(4-amino-5-chloro-2-methoxybenzamido)acetic acid 2, a metabolite of metoclopramide 1, has been accomplished through the coupling of 4-amino-5-chloro-2-methoxybenzoic acid 4 with gly...

[Lengthening of the peptide chain at the C-terminal end of a glycosylamino acid].

Carbohydr. Res. 50 , 15-22, (1976)

An O-glycodipeptide was synthesized by lengthening the peptide chain on the C-terminal side of a glycosylamino acid unit. N-(Benzyloxycarbonyl)-3-O-(2,3,4,6-tetra-O-acetyl-beta-D-glucopyranosyl)-L-thr...


More Articles

Related Compounds

  • H-Gly-ONp Hydrochloride
  • H-Gly-Sar-Sar-OH
  • H-Gly-Ala-Tyr-OH
  • H-Gly-Tyr-NH2 · HCl
  • H-Gly-D-Val-OH
  • H-Gly-DL-Nle-OMe
  • 4-((Cyclohexylamino)methyl)benzoic acid hydrochloride
  • 1-[(2,4-Dichlorophenyl)methyl]-N-(1,1-dimethylethyl)-2-methyl-1H-indole-3-methanamine
  • 2-Methoxy-6-(pyrazol-1-yl)-benzonitrile
  • 1H-3-Benzazepin-7-ol, 8-chloro-2,3,4,5-tetrahydro-5-(3-iodophenyl)-3-methyl-, (S)-
  • (4-Methyl-tetrahydro-furan-2-yl)-methanol
  • N-(1-cyanocyclopentyl)-2-[4-(4-fluorobenzenesulfonyl)-1,4-diazepan-1-yl]acetamide
  • 5-Cyclopropyl-2-methoxy-[1,2,4]triazolo[1,5-a]pyrimidin-7-ol
  • 4,5,6,7-Tetrahydrobenzo[d]isoxazole-3-carbaldehyde
  • tert-Butyl-DL-alanine
  • Methyl 3-Formyl-5,6,7,8-tetrahydroindolizine-2-carboxylate