138597-12-3

Basic information

• Product Name: Benzenepropanenitrile, b-(acetyloxy)-a-methylene-, (R)-
• CAS NO: 138597-12-3
• Molecular Formula: C12H11NO2
• Molecular Weight: 201.225
• Mol File: 138597-12-3.mol
• Article Data: 20

Chemical Properties

• CAS DataBase Reference: Benzenepropanenitrile, b-(acetyloxy)-a-methylene-, (R)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenepropanenitrile, b-(acetyloxy)-a-methylene-, (R)-(138597-12-3)
• EPA Substance Registry System: Benzenepropanenitrile, b-(acetyloxy)-a-methylene-, (R)-(138597-12-3)

Safety Data

• Hazardous Substances Data: 138597-12-3(Hazardous Substances Data)

Upstream product

• 19362-96-0 2-(1-hydroxybenzyl)acrylonitrile 
• 108-24-7 acetic anhydride 
• 75-36-5 acetyl chloride 
• 100-52-7 benzaldehyde 
• 107-13-1 acrylonitrile 

Downstream Products

• 177838-08-3 (2E)-2-(Acetoxymethyl)-3-phenylprop-2-enenitrile 
• 903563-87-1 2-aminomethyl-3-phenylacrylonitrile 
• 144453-40-7 2-benzylidene-pent-4-enenitrile 
• 849777-69-1 ethyl 2-acetyl-4-cyano-3-phenylpent-4-enoate 
• 1020667-33-7 ethyl 1-(2-cyano-1-phenylallyl)-2-oxocyclopentanecarboxylate 
• 1020666-64-1 2-(2-acetyl-3-oxo-1-phenylbutyl)acrylonitrile 
• 1072836-66-8 C₁₈H₁₃N 

Relevant articles and documents

Crystal Structure of N-(2-Cyano-1-Phenylprop-2-en-1-yl)-4-Methylbenzenesulfonamide

New allylsulfonamide is prepared in a four-step synthetic route: the Morita-Baylis-Hillman adduct prepared from benzaldehyde and acrylonitrile is acetylated using acetic anhydride and DMAP. The acetylated product reacts with DABCO displaced by the additio

A one-pot three-step multicomponent synthesis of functionalized allyl dithiocarbamates using Baylis–Hillman reaction

A one-pot, pseudo five-component, highly diastereoselective, and mild procedure for the synthesis of functionalized allyl dithiocarbamates is developed. The Baylis–Hillman (BH) reaction of aromatic (heteroaromatic) aldehydes and activated alkenes using DA

One-pot synthesis of allyl thioacetate from benzaldehydes and activated alkenes using the Morita-Baylis-Hillman reaction as a key step

An efficient, regioselective and steresoselecitive one-pot protocol for the synthesis of (Z)-S-2-alkoxycarbonyl-3-acylallyl ethanethioates and (E)-S-2-cyano-3-acylallyl ethanethioates from benzaldehydes and activated alkenes (methyl acrylate and acrylonit