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2,4-Hexadiyne,1,6-dichloro-

Base Information
  • Chemical Name:2,4-Hexadiyne,1,6-dichloro-
  • CAS No.:16260-59-6
  • Molecular Formula:C6H4 Cl2
  • Molecular Weight:147.00
  • Hs Code.:
  • Mol file:16260-59-6.mol
2,4-Hexadiyne,1,6-dichloro-

Synonyms:1,6-Dichloro-2,4-hexadiyne

Suppliers and Price of 2,4-Hexadiyne,1,6-dichloro-
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
Total 4 raw suppliers
Chemical Property of 2,4-Hexadiyne,1,6-dichloro-
Chemical Property:
  • Refractive Index:1.5610 (estimate) 
  • Boiling Point:170.62°C (rough estimate) 
  • PSA:0.00000 
  • Density:1.1792 (rough estimate) 
  • LogP:1.47080 
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):
  • Hazard Codes: 3:;
     
  • Safety Statements:An extremely shock;sensitive explosive. Upon decompositi"> −. See also CHLORINATED HYDROCARBONS, ALIPHATIC." target="_blank">An extremely shock;sensitive explosive. Upon decompositi 
MSDS Files:

SDS file from LookChem

Useful:
  • General Description **2,4-Hexadiyne,1,6-dichloro-** (also known as **1,6-Dichloro-2,4-hexadiyne**) is a diyne compound featuring chlorine substituents at the terminal positions (C1 and C6). It serves as a versatile substrate in nickel-catalyzed double SN2′ substitution reactions with Grignard reagents, yielding ene-yne-ene derivatives that are potential building blocks for conjugated polymers. 2,4-Hexadiyne,1,6-dichloro-'s reactivity highlights its utility in synthetic organic chemistry for constructing extended π-conjugated systems.
Technology Process of 2,4-Hexadiyne,1,6-dichloro-

There total 3 articles about 2,4-Hexadiyne,1,6-dichloro- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With pyridine; thionyl chloride; In diethyl ether; for 18h; Ambient temperature;
Guidance literature:
With copper acetylacetonate; iron(III)-acetylacetonate; potassium carbonate; In N,N-dimethyl-formamide; at 50 ℃; for 12h;
DOI:10.1016/j.tet.2010.04.017
Guidance literature:
DOI:10.1021/ja00868a013
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