164208-54-2

Basic information

• Product Name: Acetic acid 1-(4-chloro-phenyl)-2-cyano-allyl ester
• Synonyms: Acetic acid 1-(4-chloro-phenyl)-2-cyano-allyl ester
• CAS NO: 164208-54-2
• Molecular Weight: 235.67
• Mol File: 164208-54-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Acetic acid 1-(4-chloro-phenyl)-2-cyano-allyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Acetic acid 1-(4-chloro-phenyl)-2-cyano-allyl ester(164208-54-2)
• EPA Substance Registry System: Acetic acid 1-(4-chloro-phenyl)-2-cyano-allyl ester(164208-54-2)

Safety Data

• Hazardous Substances Data: 164208-54-2(Hazardous Substances Data)

Upstream product

• 104-88-1 4-chlorobenzaldehyde 
• 22056-04-8 2-[(4-chlorophenyl)hydroxymethyl]acrylonitrile 
• 108-24-7 acetic anhydride 
• 75-36-5 acetyl chloride 

Downstream Products

• 1020666-76-5 ethyl 2-acetyl-3-(4-chlorophenyl)-4-cyanopent-4-enoate 
• 1020667-35-9 ethyl 1-[1-(4-chlorophenyl)-2-cyanoallyl]-2-oxocyclopentanecarboxylate 
• 1020666-66-3 2-[2-acetyl-1-(4-chlorophenyl)-3-oxobutyl]acrylonitrile 
• 594835-24-2 (2E)-3-(4-chlorophenyl)-2-{[(4-methylphenyl)sulfonyl]methyl}prop-2-enenitrile 
• 1224508-65-9 methyl 6-amino-5-(4-chlorobenzyl)-2-methylnicotinate 
• 1224508-59-1 ethyl 6-amino-5-(4-chlorobenzyl)-2-methylnicotinate 
• 1186205-37-7 ethyl (Z)-5-(4-chlorophenyl)-4-cyano-2-nitropent-4-enoate 
• 1134780-68-9 C₁₈H₁₅ClN₂S₂ 
• 1134780-66-7 C₁₅H₁₇ClN₂S₂ 
• 1134780-64-5 C₁₆H₁₇ClN₂S₂ 
• 1072513-46-2 3-(4-chlorophenyl)-2-{[(2,2-dimethoxyethyl)amino]methyl}prop-2-enenitrile 
• 1072836-69-1 C₁₈H₁₂ClN 
• 1072836-53-3 C₁₈H₁₂ClN 

Relevant articles and documents

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

Synthesis of allyl aryl sulfone derivatives from Baylis-Hillman acetates in water

Various phenyl and p-tolyl allyl sulfone derivatives were prepared stereoselectively by reacting Baylis-Hillman acetates with sodium 4-R-benzenesulfinate (R=H, Me) in H2O. The reaction was very efficient in providing the corresponding sulfone d