38335-22-7

Basic information

• Product Name: Benzenepropanoic acid, 4-Methyl-.alpha.-oxo-
• Synonyms: Benzenepropanoic acid, 4-Methyl-.alpha.-oxo-;2-oxo-3-(p-tolyl)propanoic acid
• CAS NO: 38335-22-7
• Molecular Formula: C₁₀H₁₀O₃
• Molecular Weight: 178.1846
• Mol File: 38335-22-7.mol
• Article Data: 11

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Benzenepropanoic acid, 4-Methyl-.alpha.-oxo-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenepropanoic acid, 4-Methyl-.alpha.-oxo-(38335-22-7)
• EPA Substance Registry System: Benzenepropanoic acid, 4-Methyl-.alpha.-oxo-(38335-22-7)

Safety Data

• Hazardous Substances Data: 38335-22-7(Hazardous Substances Data)

Upstream product

• 201230-82-2 carbon monoxide 
• 104-82-5 4-Methylbenzyl chloride 
• 82309-33-9 4-(4-methylbenzylidene)-2-phenyloxazol-5-one 
• 461-72-3 2,4-imidazolidinedione 
• 104-87-0 4-methyl-benzaldehyde 
• 28744-88-9 5-(4-methyl-benzylidene)-imidazolidine-2,4-dione 
• 93634-59-4 (Z)-2-acetamido-3-(4-methylphenyl)-2-propenoic acid 
• 52773-84-9 p-methylphenylserine 
• 57427-79-9 (Z)-4-(4-methylbenzylidene)-2-phenyloxazol-5(4H)-one 

Downstream Products

• 1256735-87-1 (2E,2′E)-N,N′-(disulfanediylbis(ethane-2,1-diyl))bis(2-(hydroxyimino)-3-(3-methoxy-4-hydroxyphenyl)propanamide) 
• 1991-87-3 4-methyl-L-phenylalanine 
• 119-61-9 benzophenone 
• 1567951-56-7 C₁₉H₁₇NO₃ 
• 118740-13-9 3-(4-Methyl-benzyl)-1H-1,4,4a,9-tetraaza-anthracene-2,10-dione 
• 118779-03-6 6-(4-Methyl-benzyl)-3-phenylamino-2H-[1,2,4]triazin-5-one 
• 118740-02-6 6-(4-Methyl-benzyl)-3-methylsulfanyl-2H-[1,2,4]triazin-5-one 
• 87736-15-0 5-Chloro-6-(4-methyl-benzyl)-pyrazine-2,3-dicarbonitrile 
• 175897-66-2 2-hydroxy-3-(p-methylphenyl)propanoic acid 
• 128437-36-5 3-methyl-2-oxo-3-p-tolyl-butyric acid 

Relevant articles and documents

Bio-inspired enantioselective full transamination using readily available cyclodextrin

The mimics of vitamin B6-dependent enzymes that catalyzed an enantioselective full transamination in the pure aqueous phase have been realized for the first time through the establishment of a new “pyridoxal 5′-phosphate (PLP) catalyzed non-covalent cyclodextrin (CD)-keto acid inclusion complexes” system, and various optically active amino acids have been obtained.

Deracemisation of aryl substituted α-hydroxy esters using Candida parapsilosis ATCC 7330: Effect of substrate structure and mechanism

Candida parapsilosis ATCC 7330 was found to be an efficient biocatalyst for the deracemisation of aryl α-hydroxy esters (65-85% yield and 90-99% ee). A variety of aryl and aryl substituted α-hydroxy esters were synthesized to reflect steric and electronic effects on biocatalytic deracemisation. The mechanism of this biocatalytic deracemisation was found to be stereoinversion.

Synthetic and antiviral studies on certain acyclic nucleosides of 5- benzyl-6-azauracil derivatives

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