26682-99-5 | Methyl 2-amino-2-phenylacetate

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$243.00	$170.00
10g	98%	in stock	$441.00	$309.00

Description

• Catalog Number: AF32818
• Chemical Name: Methyl 2-amino-2-phenylacetate
• CAS Number: 26682-99-5
• Molecular Formula: C9H11NO2
• Molecular Weight: 165.1891
• MDL Number: MFCD01026128
• SMILES: COC(=O)C(c1ccccc1)N

Computed Properties

• Complexity: 153
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 3
• Undefined Atom Stereocenter Count: 1
• XLogP3: 0.9

Literature

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  Journal of environmental monitoring : JEM 20110101

• 3-Ethyl 2-methyl 8-bromo-2-phenyl-1,2,3,3a,4,9b-hexa-hydro-chromeno[4,3-b]pyrrole-2,3-dicarboxyl-ate.

  Acta crystallographica. Section E, Structure reports online 20101201

• Functionalization of methyl (R)-phenylglycinate through orthopalladation: C-Hal, C-O, C-N, and C-C bond coupling.

  Inorganic chemistry 20091221

• Trimethyl 5-(2-chloro-4-fluoro-phen-yl)-2-phenyl-pyrrolidine-2,3,4-tricarboxyl-ate.

  Acta crystallographica. Section E, Structure reports online 20091101

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  Journal of biotechnology 20060820

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  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

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  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