37627-41-1

Basic information

• Product Name: 2-Propenenitrile, 3-(4-chlorophenyl)-, (Z)-
• CAS NO: 37627-41-1
• Molecular Formula: C9H6ClN
• Molecular Weight: 163.606
• Mol File: 37627-41-1.mol
• Article Data: 58

Chemical Properties

• CAS DataBase Reference: 2-Propenenitrile, 3-(4-chlorophenyl)-, (Z)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propenenitrile, 3-(4-chlorophenyl)-, (Z)-(37627-41-1)
• EPA Substance Registry System: 2-Propenenitrile, 3-(4-chlorophenyl)-, (Z)-(37627-41-1)

Safety Data

• Hazardous Substances Data: 37627-41-1(Hazardous Substances Data)

Upstream product

• 50709-88-1 3-(4-chlorophenyl)-2-phenylsulfonyl-2-propenenitrile 
• 637-87-6 1-Chloro-4-iodobenzene 
• 107-13-1 acrylonitrile 
• 3018-12-0 dichloroacetonitrile 
• 104-88-1 4-chlorobenzaldehyde 
• 3252-43-5 dibromoacetonitrile 
• 372-09-8 cyanoacetic acid 
• 22563-58-2 3-(4-chloro-phenyl)-1-pyrrol-2-yl-propenone 
• 75-05-8 acetonitrile 
• 18881-60-2 bis-trimethylsilanyl-acetonitrile 
• 433231-64-2 C₂₀H₁₀F₁₂NO₂P 
• 2537-48-6 diethyl 1-cyanomethylphosphonate 
• 590-17-0 cyanomethyl bromide 
• 7605-28-9 2-(phenylsulfonyl)acetonitrile 

Downstream Products

• 82420-65-3 Amino-6 p-chlorophenyl-4 cyano-3 methoxy-2 pyridine 
• 24663-92-1 3-trans-p-chlorostyryl-4,5-dihydro-1,2,4-oxadiazole 
• 24702-65-6 3-(4-chloro-cis-styryl)-[1,2,4]oxadiazole 
• 24663-88-5 3-trans-p-chlorostyryl-1,2,4-oxadiazole 
• 51791-22-1 3-[(Z)-2-bromo-2-(4-chloro-phenyl)-vinyl]-[1,2,4]oxadiazole 
• 24654-32-8 3-[1,2-dibromo-2-(4-chloro-phenyl)-ethyl]-[1,2,4]oxadiazole 
• 51791-23-2 (Z)-3-bromo-3-(4-chlorophenyl)prop-2-enenitrile 
• 36175-63-0 3-(4-chloro-trans-styryl)-[1,2,4]oxadiazole-5-carboxylic acid ethyl ester 
• 51791-19-6 3-[1,2-dibromo-2-(4-chloro-phenyl)-ethyl]-[1,2,4]oxadiazole-5-carboxylic acid ethyl ester 
• 36175-61-8 3-(4-chloro-trans-styryl)-5-methyl-[1,2,4]oxadiazole 
• 51791-06-1 (1Z,2E)-3-(4-chlorophenyl)-N’-hydroxyprop-2-enimidamide 
• 36175-60-7 (E)-3-(4-chlorostyryl)-1,2,4-oxadiazol-5(4H)-one 
• 1392592-82-3 S-1-(4-chlorophenyl)-2-cyanoethyl thioacetate 
• 1392592-78-7 3-amino-1-(4-chlorophenyl)propane-1-sulfonic acid 

Relevant articles and documents

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Catalytic olefination of hydrazones of aromatic aldehydes with dibromoacetonitrile affords cinnamonitriles.

Selective and facile synthesis of α,β-unsaturated nitriles and amides with N-hydroxyphthalimide as the nitrogen source

The direct conversion of α,β-unsaturated aldehydes to corresponding nitriles promoted by Pd(OAc)2 and phthalic acid which was hydrolyzed from N-hydroxyphthalimide (NHPI) has been disclosed. Additionally, it was found that when water was used as the solvent, α,β-unsaturated amides was obtained as the main products in good to excellent yields. It was first reported that NHPI was utilized as the nitrogen source to synthesize α,β-unsaturated nitriles and amides from aldehydes. Control experiment demonstrated that aldehydes undergo a process of oximation and dehydration to form nitriles and amides.

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