1450-01-7

Basic information

• Product Name: Methanone, 2-furanylphenyl-, oxime, (Z)-
• CAS NO: 1450-01-7
• Molecular Formula: C11H9NO2
• Molecular Weight: 187.198
• Mol File: 1450-01-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Methanone, 2-furanylphenyl-, oxime, (Z)-(CAS DataBase Reference)
• NIST Chemistry Reference: Methanone, 2-furanylphenyl-, oxime, (Z)-(1450-01-7)
• EPA Substance Registry System: Methanone, 2-furanylphenyl-, oxime, (Z)-(1450-01-7)

Safety Data

• Hazardous Substances Data: 1450-01-7(Hazardous Substances Data)

Upstream product

• 2689-59-0 (furan-2-yl)(phenyl)methanone 
• 2067-52-9 (E)-(furan-2-yl)phenylmethanone oxime 

Downstream Products

• 4489-91-2 [2]furyl-phenyl keton-((Z)-O-acetyl oxime ) 
• 4489-96-7 [2]furyl-phenyl ketone-((Z)-O-benzoyl oxime ) 
• 102028-70-6 [2]furyl-phenyl ketone-[(Z)-O-(toluene-4-sulfonyl)-oxime ] 
• 188772-84-1 (S)-N-[(furan-2-yl)(phenyl)methyl]benzamide 
• 188772-85-2 (R)-N-[α-(2-furyl)benzyl]benzamide 
• 188772-74-9 (S)-(furan-2-yl)(phenyl)methanamine 
• 188772-75-0 (R)-(furan-2-yl)(phenyl)methanamine 
• 10419-67-7 N-[(2S)-(benzoylamino)(phenyl)]ethanoic acid 
• 875-74-1 (R)-phenylglycine 
• 2935-35-5 (S)-2-phenylglycine 
• 188772-62-5 (Z)-(furan-2-yl)(phenyl)methanone O-benzyloxime 

Relevant articles and documents

Novel enantioselective synthesis of both enantiomers of furan-2-yl amines and amino acids

A new enantioselective synthesis of furan-2-yl amines and amino acids is described, in which the key step is the oxazaborolidine-catalyzed enantioselective reduction of O-benzyl (E)- and (Z)-furan-2-yl ketone oximes to the corresponding chiral amines. The chirality of the furan-2-yl amines is fully controlled by the appropriate choice of the geometrical isomer of the O-benzyl oxime. Oxidation of the furan ring furnished amino acids in high yields.