72621-22-8

Basic information

• Product Name: Benzenaminium, 4-formyl-N,N,N-trimethyl-, bromide
• CAS NO: 72621-22-8
• Molecular Formula: C10H14NO.Br
• Molecular Weight: 244.131
• Mol File: 72621-22-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzenaminium, 4-formyl-N,N,N-trimethyl-, bromide(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenaminium, 4-formyl-N,N,N-trimethyl-, bromide(72621-22-8)
• EPA Substance Registry System: Benzenaminium, 4-formyl-N,N,N-trimethyl-, bromide(72621-22-8)

Safety Data

• Hazardous Substances Data: 72621-22-8(Hazardous Substances Data)

Upstream product

• 73000-45-0 Trimethyl-{4-[(E)-phenyliminomethyl]-phenyl}-ammonium; bromide 
• 73000-46-1 (4-{[(Z)-4-Butyl-phenylimino]-methyl}-phenyl)-trimethyl-ammonium; bromide 
• 72621-03-5 (4-{[(Z)-4-Heptyl-phenylimino]-methyl}-phenyl)-trimethyl-ammonium; bromide 
• 70987-23-4 (4-{[(E)-4-Dodecyl-phenylimino]-methyl}-phenyl)-trimethyl-ammonium; bromide 
• 74-83-9 methyl bromide 
• 100-10-7 4-dimethylamino-benzaldehyde 

Downstream Products

• 73000-46-1 (4-{[(Z)-4-Butyl-phenylimino]-methyl}-phenyl)-trimethyl-ammonium; bromide 
• 73000-45-0 Trimethyl-{4-[(E)-phenyliminomethyl]-phenyl}-ammonium; bromide 
• 72621-03-5 (4-{[(Z)-4-Heptyl-phenylimino]-methyl}-phenyl)-trimethyl-ammonium; bromide 
• 70987-23-4 (4-{[(E)-4-Dodecyl-phenylimino]-methyl}-phenyl)-trimethyl-ammonium; bromide 
• 78434-82-9 {4-[(E)-Dodecyliminomethyl]-phenyl}-trimethyl-ammonium; bromide 

Relevant articles and documents

Preparation of quarternary ammonium salt-tagged ferrocenylphosphine-imine ligands and their application to palladium-catalyzed asymmetric allylic substitution

A series of novel quarternary ammonium salt-modified chiral ferrocenylphosphine-imine ligands have been synthesized and the molecular structure of BIT5 has been determined by single-crystal X-ray diffraction. The applicability of these ligands in asymmetric C*C and C*N bond formation was demonstrated. High enantioselectivity was obtained in the Pd-catalyzed asymmetric substitution of 1,3-diphenyl- 2-propenyl acetate, with dimethyl malonate (up to 94.6% ee) and benzylamine (up to 92.6% ee).

Formation of Stable Bilayer Assemblies in Dilute Aqueous Solution from Ammonium Amphiphiles with the Diphenylazomethine Segment

Quarternary ammonium amphiphiles of the following structures were synthesized: Cn-BB-N+3C1 and Cn-BB-Cm-N+3C1, where Cn and Cm are hydrocarbon chains of n =