866102-73-0

Basic information

• Product Name: N-(4-bromophenyl)succinamide
• Synonyms: N-(4-bromophenyl)succinamide
• CAS NO: 866102-73-0
• Molecular Weight: 271.114
• Mol File: 866102-73-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-(4-bromophenyl)succinamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-bromophenyl)succinamide(866102-73-0)
• EPA Substance Registry System: N-(4-bromophenyl)succinamide(866102-73-0)

Safety Data

• Hazardous Substances Data: 866102-73-0(Hazardous Substances Data)

Upstream product

• 638-32-4 succinamic acid 
• 106-40-1 4-bromo-aniline 
• 15386-95-5 N₁-phenylsuccinamide 

Downstream Products

• 3744-18-1 N-(4-bromo-phenylcarbamoyl)-β-alanine 
• 866102-79-6 2-(dimethylamino)ethyl 4-[[(benzyloxy)carbonyl](4-{[(benzyloxy)carbonyl]amino}butyl)amino]benzoate 
• 866102-78-5 4-[[(benzyloxy)carbonyl](4-{[(benzyloxy)carbonyl]amino}butyl)amino]benzoic acid 
• 866102-80-9 2-(dimethylamino)ethyl 4-[(4-aminobutyl)amino]benzoate 
• 866102-76-3 N-[4-(acetylamino)butyl]-N-(4-cyanophenyl)acetamide 
• 866102-75-2 N-[4-(acetylamino)butyl]-N-(4-bromophenyl)acetamide 
• 866102-77-4 4-[(4-aminobutyl)amino]benzoic acid 
• 866102-74-1 N-(4-bromophenyl)butane-1,4-diamine 

Relevant articles and documents

Modifications to the tetracaine scaffold produce cyclic nucleotide-gated channel blockers with widely varying efficacies

Five new tetracaine analogues were synthesized and evaluated for potency of blockade of cyclic nucleotide-gated channels relative to a multiply charged tetracaine analogue described previously (4). Increased positive charge at the tertiary amine end of tetracaine results in higher potency and voltage dependence of block. Modifications that reduce the hydrophobic character at the butyl tail are deleterious to block. The tetracaine analogues described here have apparent affinities for CNGA1 channels that vary over nearly 8 orders of magnitude.