139413-83-5

Basic information

• Product Name: 2-Propenenitrile, 2-(bromomethyl)-3-(4-chlorophenyl)-, (E)-
• CAS NO: 139413-83-5
• Molecular Formula: C10H7BrClN
• Molecular Weight: 256.529
• Mol File: 139413-83-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-Propenenitrile, 2-(bromomethyl)-3-(4-chlorophenyl)-, (E)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propenenitrile, 2-(bromomethyl)-3-(4-chlorophenyl)-, (E)-(139413-83-5)
• EPA Substance Registry System: 2-Propenenitrile, 2-(bromomethyl)-3-(4-chlorophenyl)-, (E)-(139413-83-5)

Safety Data

• Hazardous Substances Data: 139413-83-5(Hazardous Substances Data)

Upstream product

• 104-88-1 4-chlorobenzaldehyde 
• 22056-04-8 2-[(4-chlorophenyl)hydroxymethyl]acrylonitrile 

Downstream Products

• 1415645-82-7 (Z)-3-(4-chlorophenyl)-2-((5-oxo-4-(4-(trifluoromethyl)phenyl)-4,5-dihydro-1H-tetrazol-1-yl)methyl)acrylonitrile 
• 1373931-21-5 (E)-3-(4-chlorophenyl)-2-({2-[(E)-(hydroxyimino)methyl]phenoxy}methyl)acrylonitrile 
• 1010396-76-5 C₁₇H₁₂NO₂Cl 

Relevant articles and documents

Efficient synthesis of N-allylated 2-nitroiminoimidazolidine analogues from Baylis–Hillman bromides

Various Baylis–Hillman–derived new N-allylated 2-nitroiminoimidazolidine analogs were efficiently prepared using potassium carbonate as base. Simple workup procedure, excellent yields, and mild reaction conditions are the salient features of this method. All the synthesized compounds are screened for their larvicidal activity on fourth instar mosquito larvae, Culex quinquefasciatus.

Mild and practical stereoselective synthesis of (Z)- and (E)-allyl bromides from Baylis-Hillman adducts using Appel agents (PPh3/CBr4): a facile synthesis of semiplenamides C and E

Appel agents (PPh3/CBr4) have been utilized for high-yielding stereoselective synthesis of (Z)- and (E)-allyl bromides from Baylis-Hillman adducts at room temperature. The method has been applied for the synthesis of naturally occurr