99033-96-2

Basic information

• Product Name: Benzenepropanoic acid, a-(hydroxyimino)-, (Z)-
• CAS NO: 99033-96-2
• Molecular Formula: C9H9NO3
• Molecular Weight: 179.175
• Mol File: 99033-96-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Benzenepropanoic acid, a-(hydroxyimino)-, (Z)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenepropanoic acid, a-(hydroxyimino)-, (Z)-(99033-96-2)
• EPA Substance Registry System: Benzenepropanoic acid, a-(hydroxyimino)-, (Z)-(99033-96-2)

Safety Data

• Hazardous Substances Data: 99033-96-2(Hazardous Substances Data)

Upstream product

• 5740-34-1 3-phenyl-2-sulfanylpropenoic acid 
• 156-06-9 2-oxo-3-(phenyl)propionic acid 
• 5440-25-5 3-(hydroxyimino)-4-phenylbutan-2-one 
• 6943-96-0 ethyl 2-(hydroxyimino)-3-phenylpropanoate 
• 616-75-1 2-benzylmalonic acid 
• 7664-93-9 sulfuric acid 
• 7732-18-5 water 
• 620-79-1 Ethyl 2-benzylacetoacetate 
• 6731-58-4 ethyl 2-cyano-3-phenylpropanoate 
• 1155-48-2 2-benzoylaminocinnamic acid 
• 7664-41-7 ammonia 
• 64-17-5 ethanol 
• 5416-07-9 3-phenyl-2-thioxopropanoic acid 
• 7803-49-8 hydroxylamine 

Downstream Products

• 150-30-1 Phenylalanine 
• 75389-00-3 3,4-dibenzyl-1,2,5-oxadiazole-2-oxide 
• 140-29-4 phenylacetonitrile 
• 156-06-9 2-oxo-3-(phenyl)propionic acid 
• 148983-84-0 [Cu((C₆H₅CH₂C(NO)COO))(C₅H₅N)2H₂O] 
• 264607-24-1 3-benzyl-5-phenyl-4,5-dihydroisoxazole 
• 177612-82-7 [Pt(O₂CC(CH₂C₆H₅)NO)(C₂₆H₂₄P₂)]*CHCl₃ 
• 155209-26-0 {((CH₃)((CH₃)2CH)C₆H₄)RuCl(O₂CC(CH₂C₆H₅)NOH)} 
• 408539-45-7 2-benzyloxyimino-3-phenyl-propionyl chloride 
• 35031-43-7 2-benzyloxyimino-3-phenylpropionic acid 
• 91133-67-4 2-ethoxyimino-3-phenylpropionic acid 
• 6362-66-9 4-phenyl-dihydro-furan-2,3-dione 

Relevant articles and documents

Visible-light-mediated generation of nitrile oxides for the photoredox synthesis of isoxazolines and isoxazoles

Visible-light photoredox catalysis enables the synthesis of biologically relevant isoxazolines and isoxazoles from hydroxyimino acids. The process shows broad functional group compatibility and mechanistic and computational studies support a visible-light-mediated generation of nitrile oxides by two sequential oxidative single electron transfer processes.