857624-43-2

Basic information

• Product Name: Acetanilide, p-(2-cyanoethyl)- (4CI)
• Synonyms: Acetanilide, p-(2-cyanoethyl)- (4CI)
• CAS NO: 857624-43-2
• Molecular Formula: C11H12N2O
• Molecular Weight: 188.22578
• Mol File: 857624-43-2.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Acetanilide, p-(2-cyanoethyl)- (4CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Acetanilide, p-(2-cyanoethyl)- (4CI)(857624-43-2)
• EPA Substance Registry System: Acetanilide, p-(2-cyanoethyl)- (4CI)(857624-43-2)

Safety Data

• Hazardous Substances Data: 857624-43-2(Hazardous Substances Data)

Upstream product

• 122-85-0 para-acetamidobenzaldehyde 
• 101251-09-6 (4-acetylaminophenyl)boronic acid 
• 107-13-1 acrylonitrile 

Relevant articles and documents

A Titanium-Catalyzed Reductive α-Desulfonylation

A titanium(III)-catalyzed desulfonylation gives access to functionalized alkyl nitrile building blocks from α-sulfonyl nitriles, circumventing traditional base-mediated α-alkylation conditions and strong single electron donors. The reaction tolerates numerous functional groups including free alcohols, esters, amides, and it can be applied also to the α-desulfonylation of ketones. In addition, a one-pot desulfonylative alkylation is demonstrated. Preliminary mechanistic studies indicate a catalyst-dependent mechanism involving a homolytic C?S cleavage.

A strategy for generating aryl radicals from arylborates through organic photoredox catalysis: Photo-Meerwein type arylation of electron-deficient alkenes

Photoinduced reactions of arylboronic acids with electron deficient alkenes under mild organic photoredox catalysis conditions lead to the formation of Meerwein arylation type adducts via the generation of aryl radicals.