3737-00-6

Basic information

• Product Name: (E)-3-bromo-1-chloro-prop-1-ene
• Synonyms: 3-Bromo-1-chloro-1-propene;Bromochloropropene;CBP-55;1-Chloro-3-bromo-1-propene
• CAS NO: 3737-00-6
• Molecular Formula: C₃H₄BrCl
• Molecular Weight: 155.42
• Mol File: 3737-00-6.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 141.9°Cat760mmHg
• Flash Point: 37.3°C
• Appearance: /
• Density: 1.614
• Vapor Pressure: 7.17mmHg at 25°C
• Refractive Index: 1.505
• CAS DataBase Reference: (E)-3-bromo-1-chloro-prop-1-ene(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-3-bromo-1-chloro-prop-1-ene(3737-00-6)
• EPA Substance Registry System: (E)-3-bromo-1-chloro-prop-1-ene(3737-00-6)

Safety Data

• Hazardous Substances Data: 3737-00-6(Hazardous Substances Data)

Usage

Hazard

A poison by ingestion. Low toxicity by inhalation. Human systemic effects.

Safety Profile

A poison by ingestion. Low toxicity by inhalation. Human systemic effects. When heated to decomposition it emits toxic vapors of Brand Cl-.

InChI:InChI=1/C3H4BrCl/c4-2-1-3-5/h1,3H,2H2/b3-1+

Upstream product

• 506-68-3 bromocyane 
• 86865-63-6 (3-chloro-allyl)-methyl-amine 
• 542-75-6 E/Z-1,3-Dichloropropene 
• 590-21-6 propenyl chloride 
• 67-66-3 chloroform 
• 54410-95-6 (3-chloro-allyl)-phenyl ether 
• 7726-95-6 bromine 

Downstream Products

• 29516-63-0 2-((E)-3-Chloro-allyloxy)-1-methyl-3,5-dinitro-benzene 
• 91166-39-1 (E)-penta-2,4-dien-1-ylbenzene 
• 77131-99-8 2-Benzyl-3-vinyl-oxirane 
• 132637-79-7 (E)-5-Chloro-1-phenyl-pent-4-en-2-ol 
• 132637-75-3 3-Chloro-1-phenyl-pent-4-en-2-ol 

Relevant articles and documents

Synthese d'epoxydes vinyliques halogenes

β-Halovinyloxiranes 2-9, a little studies class of compounds, have been synthesized by condensation of haloallylsulfonium ylids derived from salts 1 with aliphatic, aromatic or α,β-unsaturated aldehydes in a two-phase system (aqueous sodium hydroxide and methylene chloride).The best yields were obtained when the reaction was carried out at room temperature with two or three equivalents of sodium hydroxide.Moreover, α-halovinyloxiranes 13-15 have been prepared by addition of the ylids derived from vinyl and benzylsulfonium salts 10-12 to α-halounsaturated aldehydes.