2852-07-5

Usage

Safety Profile

Moderately toxic by ingestion andinhalation. An eye irritant. When heated to decompositionit emits toxic fumes of Clí.

InChI:InChI=1/C4H3Cl3/c1-2-3(5)4(6)7/h2H,1H2

Upstream product

• 92334-03-7 trimethyl-(3,3,4,4-tetrachloro-butyl)-ammonium; iodide 
• 40589-38-6 4-chloro-but-1-en-3-yne 
• 3345-66-2 α-methyltrichloroallyl alcohol 
• 3574-42-3 1,1,2,4-tetrachloro-2-butene 
• 34867-74-8 1,1,2,2,4-pentachlorobutane 
• 3266-36-2 3,3,4,4-tetrachloro-butan-2-ol 
• 22336-56-7 1,1,2,4-tetrachloro-but-1-ene 

Downstream Products

• 16427-18-2 (3,4,4-Trichlor-but-3-enyl)-phenyl-sulfid 
• 94796-73-3 cis-1,1,2,4-tetrachloro-1,3-butadiene 
• 52704-84-4 1,1,2,3,4-pentachloro-1-butene 

Related news

Copolymers of dimethyl 2-methyl-1,3-butadienethiophosphonate with 1,1,2-TRICHLORO-1,3-BUTADIENE (cas 2852-07-5) or ethyl α-cyanoacrylate07/12/2019

Dimethyl 2-methyl-1,3-butadienethiophosphonate was copolymerized radically with 1,1,2-trichloro-1,3-butadiene or with ethyl α-cyanoacrylate. IR and NMR spectra (1H and 31P) give evidence that polymerization of the phosphorus-containing monomer and, when it is present in excess, also its copolym...detailed

Relevant academic research and scientific papers

Dehydration of halogenated, unsaturated alcohols to form halogenated, conjugated dienes

Halogenated, unsaturated alcohols are dehydrated by contacting the alcohol and a carrier gas with a silica alumina catalyst to form dienes of the formula: STR1 wherein each X is independently hydrogen, fluorine chlorine, or bromine with the proviso that no more than one of them is hydrogen, and each R is independently hydrogen, alkyl, aralkyl, alkaryl, or aryl.

CHEMISTRY OF DIENES AND THEIR DERIVATIVES. XVII. LOW-TEMPERATURE CHLORINATION OF 2-CHLORO- AND 1,2-DICHLORO-1,3-BUTADIENES IN THE PRESENCE OF AN INHIBITOR OF RADICAL REACTIONS

During the chlorination of chloroprene (80-85percent conversion) in carbon tetrachloride at -5 to 0 deg C in the presence of tert-butylpyrocatechol 1,2-dichloro-1,3-butadiene, 3,3,4-trichloro-1-butene, 2,3,4-trichloro-1-butene, and 1,2,4-trichloro-2-butene are formed in percentage ratios of 20.4:6.7:3.4:69.5.During chlorination to total conversion of chloroprene under these conditions a series of other compounds are also formed as a result of the further chlorination of 1,2-dichloro-1,3-butadiene and 3,3,4-trichloro-1-butene.During the chlorination of 1,2-dichloro-1,3-butadiene to a high degree of conversion 1,2,4-trichloro-1,3-butadiene, 1,2,3,4-tetrachloro-1-butene, and 1,1,2,4-tetrachloro-2-butene are formed in ratios of 11.4:49:39.6.