101414-14-6

Basic information

• Product Name: 1,1,2,4,5,6-hexachloro-1,4-hexadiene
• Synonyms: 1,1,2,4,5,6-hexachloro-1,4-hexadiene
• CAS NO: 101414-14-6
• Molecular Weight: 288.816
• Mol File: 101414-14-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1,1,2,4,5,6-hexachloro-1,4-hexadiene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1,2,4,5,6-hexachloro-1,4-hexadiene(101414-14-6)
• EPA Substance Registry System: 1,1,2,4,5,6-hexachloro-1,4-hexadiene(101414-14-6)

Safety Data

• Hazardous Substances Data: 101414-14-6(Hazardous Substances Data)

Upstream product

• 21400-25-9 1,1,2-trichloropropene 
• 882-33-7 diphenyldisulfane 

Relevant articles and documents

FREE-RADICAL REACTIONS OF 1,1,2-TRICHLOROPROPENE. III. FREE-RADICAL THIYLATION OF TRICHLOROPROPENE BY DIARYL DISULFIDES

The reaction of CCl2=CClCH3 with ArSSAr (Ar = 4-ClC6H4, C6H5, 4-CH3C6H4), initiated by UV irradiation, in a quartz flask leads to the formation of a mixture of isomeric sulfides ArSC(CH3)=CCl2 and cis- and trans-ArSCCl=CClCH3 and also the sulfides ArSCH2CCl=CCl2 and ArSCCl2CCl2CH3.In addition, significant amounts of the products from oxidation and oligomerization of trichloropropene CH3CCl2COOH, CCl2=CClCH2CCl=CClCH2Cl, and CCl2=CClCH2CCl2CCl2CH3 are formed.The oligomerization of trichloropropene is almost completely suppressed in molybdenum glass.A reaction mechanism involving the formation of the radicals ArSC(CH3)ClC.Cl2 and ArSCCl2C.ClCH3 and the allyl radical .CH2CCl=CCl2 is proposed.