H-D-Phg-OMe.HCl
Suppliers
Names
[ CAS No. ]:
19883-41-1
[ Name ]:
H-D-Phg-OMe.HCl
[Synonym ]:
(S)-2-PHENYLGLYCINE METHYL ESTER HYDROCHLORIDE
methyl (2S)-amino(phenyl)ethanoate hydrochloride (1:1)
D-phenylglycine methyl ester hydrochloride
Benzeneacetic acid, α-amino-, methyl ester, (αR)-, hydrochloride (1:1)
METHYL (2R)-2-AMINO-2-PHENYLACETATE HYDROCHLORIDE
EINECS 243-399-9
H-PH-Phg-Ome hydrochloride
S)-(+)-2-Phenylglycine methyl ester hydrochloride
D-Phenylycine Methyl Ester Hydrichloride
H-D-PHG-OME HCL
(R)-PGME hydrochloride
L-Phenylglycine methyl ester hydrochloride
Benzeneacetic acid, α-amino-, methyl ester, (αS)-, hydrochloride (1:1)
H-D-Phg-OMe.HCl
(S)-Methyl 2-amino-2-phenylacetate hydrochloride
H-PHG-OME HCL
(R)-Methyl 2-amino-2-phenylacetate hydrochloride
(S)-a-Amino-benzeneacetic acid methyl ester HCl
D-Phg-OMe*HCl
Methyl (2S)-amino(phenyl)acetate hydrochloride (1:1)
D-phenylglycine methyl ester ·HCl
L-Phenylglycine methylester hydrochloride
Methyl (2R)-amino(phenyl)acetate hydrochloride (1:1)
(R)-(-)-2-Phenylglycine Methyl Ester Hydrochloride
(R)-(−)-2-Phenylglycine methyl ester hydrochloride
(S)-(+)-2-Phenylglycine methyl ester hydrochloride
MFCD00137487
H-D-Phg-OMe.HCl
Chemical & Physical Properties
[ Density]:
1.126g/cm3
[ Boiling Point ]:
238.9ºC at 760mmHg
[ Melting Point ]:
189-191 °C(lit.)
[ Molecular Formula ]:
C9H12ClNO2
[ Molecular Weight ]:
201.650
[ Flash Point ]:
104.7ºC
[ Exact Mass ]:
201.055649
[ PSA ]:
52.32000
[ LogP ]:
2.36170
[ Vapour Pressure ]:
0.0412mmHg at 25°C
[ Storage condition ]:
2~8°C
Safety Information
[ Symbol ]:
GHS07
[ Signal Word ]:
Warning
[ Hazard Statements ]:
H319
[ Precautionary Statements ]:
P305 + P351 + P338
[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves
[ Hazard Codes ]:
Xi: Irritant;
[ Risk Phrases ]:
R36
[ Safety Phrases ]:
S26-S36/37
[ RIDADR ]:
NONH for all modes of transport
[ WGK Germany ]:
3
Synthetic Route
Precursor & DownStream
Precursor
DownStream
Articles
Biotechnol. Lett. 25(6) , 461-4, (2003)
Lipase-catalyzed enantioselective ammonolysis of phenylglycine methyl ester was processed by in situ racemization with ammonium carbamate as the acyl acceptor. Using 1 mM benzaldehyde or 0.6 mM chloro...
Biotechnol. Appl. Biochem. 38(Pt 2) , 107-10, (2003)
Ammonium, provided by ammonium carbamate as a novel acyl acceptor, was adopted for enzymic enantioselective ammonolysis of racemic phenylglycine methyl ester in this paper and it has been found that t...
Biochemistry. (Mosc.) 65(12) , 1367-75, (2000)
Kinetic regularities of the enzymatic acyl group transfer reactions have been studied using ampicillin synthesis catalyzed by E. coli penicillin acylase as an example. It was shown that ampicillin syn...