Home Aminos (S)-Methyl 2-amino-2-phenylacetate

(S)-Methyl 2-amino-2-phenylacetate

CAS No.:
37760-98-8
Catalog Number:
AG00CLLQ
Molecular Formula:
C9H11NO2
Molecular Weight:
165.1891
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
250mg
96%
In Stock USA
United States
$62
- +
1g
96%
In Stock USA
United States
$100
- +
5g
96%
In Stock USA
United States
$375
- +
10g
96%
In Stock USA
United States
$688
- +
Product Description
Catalog Number:
AG00CLLQ
Chemical Name:
(S)-Methyl 2-amino-2-phenylacetate
CAS Number:
37760-98-8
Molecular Formula:
C9H11NO2
Molecular Weight:
165.1891
MDL Number:
MFCD11978063
IUPAC Name:
methyl (2S)-2-amino-2-phenylacetate
InChI:
InChI=1S/C9H11NO2/c1-12-9(11)8(10)7-5-3-2-4-6-7/h2-6,8H,10H2,1H3/t8-/m0/s1
InChI Key:
BHFLUDRTVIDDOR-QMMMGPOBSA-N
SMILES:
COC(=O)[C@H](c1ccccc1)N
UNII:
HFS522G80L
Properties
Complexity:
153  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Defined Bond Stereocenter Count:
0
Exact Mass:
165.079g/mol
Formal Charge:
0
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
165.192g/mol
Monoisotopic Mass:
165.079g/mol
Rotatable Bond Count:
3  
Topological Polar Surface Area:
52.3A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.9  
Literature
Title Journal
Life cycle assessment of solar photo-Fenton and solar photoelectro-Fenton processes used for the degradation of aqueous α-methylphenylglycine. Journal of environmental monitoring : JEM 20110101
Functionalization of methyl (R)-phenylglycinate through orthopalladation: C-Hal, C-O, C-N, and C-C bond coupling. Inorganic chemistry 20091221
NMDA receptor affinities of 1,2-diphenylethylamine and 1-(1,2-diphenylethyl)piperidine enantiomers and of related compounds. Bioorganic & medicinal chemistry 20090501
Coupling solar photo-Fenton and biotreatment at industrial scale: main results of a demonstration plant. Journal of hazardous materials 20070731
Life cycle assessment of a coupled solar photocatalytic-biological process for wastewater treatment. Water research 20061101
Efficient enantioselective hydrolysis of D,L-phenylglycine methyl ester catalyzed by immobilized Candida antarctica lipase B in ionic liquid containing systems. Journal of biotechnology 20060820
Amine degradation by 4,5-epoxy-2-decenal in model systems. Journal of agricultural and food chemistry 20060322
Stereoselective acylation of a racemic amine with C(alpha)-methyl phenylglycine-based dipeptide 5(4H)-oxazolones. Chirality 20051001
Determination of the absolute configuration of Anisotome irregular diterpenes: application of CD and NMR methods. Chirality 20041001
Increasing the synthetic performance of penicillin acylase PAS2 by structure-inspired semi-random mutagenesis. Protein engineering, design & selection : PEDS 20040701
A novel chiral terpyridine macrocycle as a fluorescent sensor for enantioselective recognition of amino acid derivatives. Chemical communications (Cambridge, England) 20040221
Lipase-catalysed enantioselective ammonolysis of phenylglycine methyl ester in organic solvent. Biotechnology and applied biochemistry 20031001
Enhanced enzymatic synthesis of a semi-synthetic cephalosprin, cefaclor, with in situ product removal. Biotechnology letters 20030701
Improving lipase-catalyzed enantioselective ammonolysis of phenylglycine methyl ester in organic solvent by in situ racemization. Biotechnology letters 20030301
[Three dimensional structure analysis of organic chemical compounds from natural sources using NMR spectral analysis]. Kokuritsu Iyakuhin Shokuhin Eisei Kenkyujo hokoku = Bulletin of National Institute of Health Sciences 20030101
[Lipase-catalyzed enantioselective ammonolysis of racemic phenylglycine methyl ester in organic solvent]. Sheng wu gong cheng xue bao = Chinese journal of biotechnology 20020101
Biotransformations catalyzed by multimeric enzymes: stabilization of tetrameric ampicillin acylase permits the optimization of ampicillin synthesis under dissociation conditions. Biomacromolecules 20010101
Properties