57418-97-0

Basic information

• Product Name: 4-BROMO-3-CHLOROBENZONITRILE
• Synonyms: 4-BROMO-3-CHLOROBENZONITRILE;Chloro-4- bromobenzonitrile
• CAS NO: 57418-97-0
• Molecular Formula: C₇H₃BrClN
• Molecular Weight: 216.47
• Mol File: 57418-97-0.mol
• Article Data: 4

Chemical Properties

• Melting Point: 80-81℃
• Boiling Point: 261℃
• Flash Point: 112℃
• Appearance: /
• Density: 1.74
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 4-BROMO-3-CHLOROBENZONITRILE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-BROMO-3-CHLOROBENZONITRILE(57418-97-0)
• EPA Substance Registry System: 4-BROMO-3-CHLOROBENZONITRILE(57418-97-0)

Safety Data

• Hazardous Substances Data: 57418-97-0(Hazardous Substances Data)

Usage

Chemical Properties

off-white crystalline

Upstream product

• 21803-75-8 4-amino-3-chlorobenzonitrile 
• 72635-78-0 3-amino-4-bromobenzonitrile 

Downstream Products

• 914106-28-8 3-chloro-4-[2-(trimethylsilyl)ethynyl]benzonitrile 
• 914106-31-3 3-chloro-4-(3-hydroxy-3-methylbut-1-ynyl)benzonitrile 
• 1308279-93-7 thyl (E)-4-Bromo-3-chlorocinnamate 
• 1261878-70-9 ethyl 3-(4-bromo-3-chlorophenyl)propanoate 
• 1308280-00-3 ethyl 3-[4-(3'-(1-adamantyl)-4'-benzyloxyphenyl)-3-chlorophenyl]propanoate 
• 1308280-06-9 ethyl 3-[4-(3'-(1-adamantyl)-4'-hydroxy)-3-chlorophenyl]propanoate 
• 1308280-12-7 3-[4-(3'-(1-adamantyl)-4'-hydroxy)-3-chlorophenyl]propionic acid 
• 120077-69-2 3-chloro4-bromo-benzaldehyde 
• 1616603-72-5 3-benzyl-2-oxo-2,3-dihydro-1H-benzo[d]imidazole-5-carbonitrile 
• 945391-06-0 3-chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrile 
• 1208076-65-6 (4‐bromo‐3‐chlorophenyl)methanamine 

Relevant articles and documents

Heteroatom-substituted analogues of orphan nuclear receptor small heterodimer partner ligand and apoptosis inducer (E)-4-[3-(1-adamantyl)-4- hydroxyphenyl]-3-chlorocinnamic acid

(E)-4-[3'-(1-Adamantyl)-4'-hydroxyphenyl]-3-chlorocinnamic acid (3-Cl-AHPC) induces the cell cycle arrest and apoptosis of cancer cells. Because its pharmacologic properties-solubility, bioavailability, and toxicity-required improvement for translation, s

Synthesis and antiprotozoal activity of dicationic 3,5-diphenylisoxazoles

Novel dicationic 3,5-diphenylisoxazole compounds are described. Synthetic routes to these novel compounds are provided. Several of the compounds displayed in vitro activity versus Trypanosoma brucei brucei and Plasmodium falciparum comparable to that of furamidine. A majority of the novel compounds also were less toxic to VERO cells than furamidine.