109346-98-7

Basic information

• Product Name: Benzonitrile, 3-(2-oxoethyl)-
• CAS NO: 109346-98-7
• Molecular Formula: C9H7NO
• Molecular Weight: 145.161
• Mol File: 109346-98-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Benzonitrile, 3-(2-oxoethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzonitrile, 3-(2-oxoethyl)-(109346-98-7)
• EPA Substance Registry System: Benzonitrile, 3-(2-oxoethyl)-(109346-98-7)

Safety Data

• Hazardous Substances Data: 109346-98-7(Hazardous Substances Data)

Upstream product

• 956526-81-1 m-cyano-2-methoxyvinylbenzene 

Downstream Products

• 193290-27-6 3-(2-hydroxyethyl)benzonitrile 
• 484065-64-7 3-(2-chloroethyl)benzonitrile 
• 484065-65-8 2-(3-cyanophenyl)-N-{4-[(4-piperidyl)oxy]phenyl}ethanesulfonamide 
• 433230-52-5 (3-{(4R,5S)-2-Acetoxy-5-[(E)-(S)-4-(3-cyano-phenyl)-3-hydroxy-but-1-enyl]-4-hydroxy-cyclopent-1-enylsulfanyl}-propylsulfanyl)-acetic acid methyl ester 
• 1052221-35-8 3-((4-(4-fluorophenyl)-5-(2-(methylthio)-pyrimidin-4-yl)-1H-imidazol-2-yl)methyl)benzonitrile 
• 1239466-31-9 C₂₆H₁₉N₅O 
• 1237061-28-7 3-((1-hydroxy-4-(6-methylpyridin-2-yl)-5-(quinolin-6-yl)-1H-imidazol-2-yl)methyl)benzonitrile 
• 1237061-30-1 3-((1-hydroxy-5-(6-methylpyridin-2-yl)-4-(1,5-naphthyridin-2-yl)-1H-imidazol-2-yl)methyl)benzonitrile 
• 1352610-23-1 3-((4-([1,2,4]triazolo[1,5-a]pyridin-6-yl)-5-(6-methylpyridin-2-yl)-1H-imidazol-2-yl)methyl)benzonitrile 

Relevant articles and documents

Synthesis method of phenylacetaldehyde derivative

The present invention discloses a synthesis method of phenylacetaldehyde derivative, a benzaldehyde derivative is adopted as a raw material, an intermediate 2-methoxyvinylphenyl derivative is obtained through synthesis, then the phenylacetaldehyde derivative is obtained through synthesis, and the substituent group R of the benzaldehyde derivative includes but is not limited to m-methyl, m-ethyl, m-nitrile group, p-methyl, o-methyl, o-nitro and 2, 6-dimethyl. The synthesis process is simple, synthesis conditions are mild, post-treatment is relatively simple, and industrial production is easy; the universality is good, and substrates with different functional groups are compatible; the yield is considerable, part of compounds are almost quantitatively converted, and the requirement of atom economy is met.