Name: Name:2-Oxo-4-phenylbutyric acid
Brand: AABLOCKS
SKU: AA00IC1N
Rating: 90 (10 reviews)

Technical Information

Catalog Number: AA00IC1N

Chemical Name: 2-Oxo-4-phenylbutyric acid

CAS Number: 710-11-2

Molecular Formula: C10H10O3

Molecular Weight: 178.1846

MDL Number: MFCD00969471

SMILES: O=C(C(=O)O)CCc1ccccc1

Properties

Complexity: 192

Covalently-Bonded Unit Count: 1

Heavy Atom Count: 13

Hydrogen Bond Acceptor Count: 3

Hydrogen Bond Donor Count: 1

Rotatable Bond Count: 4

XLogP3: 1.6

Literature fold

Title: Direct asymmetric hydrogenation of 2-oxo-4-arylbut-3-enoic acids.

Journal: The Journal of organic chemistry20100903

Title: Simultaneous synthesis of 2-phenylethanol and L-homophenylalanine using aromatic transaminase with yeast Ehrlich pathway.

Journal: Biotechnology and bioengineering20090401

Title: Asymmetrically simultaneous synthesis of L-homophenylalanine and N6-protected-2-oxo-6-amino-hexanoic acid by engineered Escherichia coli aspartate aminotransferase.

Journal: Biotechnology progress20090101

Title: Synthesis of enantiopure (S)-2-hydroxyphenylbutanoic acid using novel hydroxy acid dehydrogenase from Enterobacter sp. BK2K.

Journal: Biotechnology progress20070101

Title: Biotransformation of R-2-hydroxy-4-phenylbutyric acid by D-lactate dehydrogenase and Candida boidinii cells containing formate dehydrogenase coimmobilized in a fibrous bed bioreactor.

Journal: Biotechnology and bioengineering20051020

Title: Asymmetrical synthesis of L-homophenylalanine using engineered Escherichia coli aspartate aminotransferase.

Journal: Biotechnology progress20050101

Title: Discovery of alpha,gamma-diketo acids as potent selective and reversible inhibitors of hepatitis C virus NS5b RNA-dependent RNA polymerase.

Journal: Journal of medicinal chemistry20040101

Title: Asymmetric synthesis of L-homophenylalanine by equilibrium-shift using recombinant aromatic L-amino acid transaminase.

Journal: Biotechnology and bioengineering20030720

Title: Use of a pharmacophore model to discover a new class of influenza endonuclease inhibitors.

Journal: Journal of medicinal chemistry20030327

Title: Inhibition of cap (m7GpppXm)-dependent endonuclease of influenza virus by 4-substituted 2,4-dioxobutanoic acid compounds.

Journal: Antimicrobial agents and chemotherapy19941201

710-11-2 | 2-Oxo-4-phenylbutyric acid