32328-81-7

Basic information

• Product Name: 4-bromo-N-methylen-aniline
• Synonyms: 4-bromo-N-methylen-aniline
• CAS NO: 32328-81-7
• Molecular Weight: 184.035
• Mol File: 32328-81-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 4-bromo-N-methylen-aniline(CAS DataBase Reference)
• NIST Chemistry Reference: 4-bromo-N-methylen-aniline(32328-81-7)
• EPA Substance Registry System: 4-bromo-N-methylen-aniline(32328-81-7)

Safety Data

• Hazardous Substances Data: 32328-81-7(Hazardous Substances Data)

Upstream product

• 131182-52-0 1,2-bis(p-bromophenylazo)cyclohexene 
• 1750-23-8 4-bromo-N-[(E)-phenylmethylidene]aniline 
• 60144-26-5 formaldehyde N,N-tetramethylenehydrazone 
• 102310-99-6 1,3,5-tri-p-bromophenyl-hexahydro-1,3,5-triazine 

Downstream Products

• 1643531-64-9 (E)-tert-butyl 3-[N-(4-bromophenyl)-N-(methyl)amino]acrylate 
• 6911-87-1 4-bromo-N-methylaniline 
• 35452-54-1 4’-bromo-N-methylformanilide 
• 1227500-99-3 C₁₃H₁₄BrNO 

Relevant articles and documents

An enantioselective chiral Bronsted acid catalyzed imino-azaenamine reaction

(Chemical Equation Presented) The enantioselective Bronsted acid catalyzed addition of methyleneaminopyrrolidine to N-Boc imines has been achieved in the presence of chiral phosphoric acids derived from 3,3′-di(phenanthryl)-H8-BINOL. The corresponding ami

Revisitation of Formaldehyde Aniline Condensation. VII. 1,3,5-Triarylhexahydro-sym-triazines and 1,3,5,7-Tetraaryl-1,3,5,7-tetrazocines from Aromatic Amines and Paraformaldehyde

A product study of the reaction between a number of aromatic amines substituted with widely different groups and paraformaldehyde in inert solvents was performed and found to yield 1,3,5-triaryl-1,3,5-hexahydrotriazines, 1,3,5,7-tetraaryl-1,3,5,7-tetrazocines and formaminals.It was not possible to correlate the product outcomes with the actual structure of the amine substrate.The X-ray diffraction structural determination of 1,3,5-tri-(t-butylphenyl)- (1b) and 1,3,5-tri-(m-fluorophenyl)-1,3,5-hexahydrotriazine (1c) showed the diaxial arrangement of the N-substituents.