72524-50-6

Basic information

• Product Name: 1,3-Cyclohexadiene, 5-(bromomethyl)-1,2,3,4-tetrachloro-
• CAS NO: 72524-50-6
• Molecular Formula: C7H5BrCl4
• Molecular Weight: 310.833
• Mol File: 72524-50-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1,3-Cyclohexadiene, 5-(bromomethyl)-1,2,3,4-tetrachloro-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Cyclohexadiene, 5-(bromomethyl)-1,2,3,4-tetrachloro-(72524-50-6)
• EPA Substance Registry System: 1,3-Cyclohexadiene, 5-(bromomethyl)-1,2,3,4-tetrachloro-(72524-50-6)

Safety Data

• Hazardous Substances Data: 72524-50-6(Hazardous Substances Data)

Upstream product

• 72448-17-0 2,3,4,5-tetrachlorothiophene-1,1-dioxide 
• 106-95-6 allyl bromide 

Downstream Products

• 1006-32-2 2,3,4,5-tetrachloro-toluene 

Relevant articles and documents

Annelations with Tetrachlorothiophene 1,1-Dioxide

Tetrachlorothiophene 1,1-dioxide is a reactive, cheletropic Diels-Alder reagent.It has been used to annelate, with loss of sulfur dioxide, a large variety of olefinic compounds to form 1,2,3,4-tetrachloro-1,3-cyclohexadiene derivatives.Dehydrochlorination of these forms 1,2,4-trichloro aromatic compounds.Both double bonds in thiophene and N-methylpyrrole are annelated.Addition of tetrachlorothiophene dioxide to acyclic 1,5-dienes, which may contain a heteroatom, provides a facile synthesis of tetrachloroisotwistenes (51) and heteroisotwistenes (56) by a double Diels-Alder reaction.Acyclic 1,6-dienes lead to tetrachlorohomoisotwistene (59) and heterohomoisotwistenes (61).By use of 1,5-cyclooctadiene, sym-dibenzocyclooctatetraene, and 1,5-cyclononadiene, the more complex carbocycles 62, 65, and 66 are generated.Tetrabromothiophene dioxide reacts like the tetrachloro compound.