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Benzene, 2-chloro-1-ethynyl-4-fluoro-

Base Information Edit
  • Chemical Name:Benzene, 2-chloro-1-ethynyl-4-fluoro-
  • CAS No.:1057670-02-6
  • Molecular Formula:C8H4ClF
  • Molecular Weight:154.571
  • Hs Code.:
  • Mol file:1057670-02-6.mol
Benzene, 2-chloro-1-ethynyl-4-fluoro-

Synonyms:Benzene, 2-chloro-1-ethynyl-4-fluoro-

Suppliers and Price of Benzene, 2-chloro-1-ethynyl-4-fluoro-
Supply Marketing:Edit
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
  • American Custom Chemicals Corporation
  • 2-CHLORO-1-ETHYNYL-4-FLUOROBENZENE 95.00%
  • 5MG
  • $ 495.33
Total 6 raw suppliers
Chemical Property of Benzene, 2-chloro-1-ethynyl-4-fluoro- Edit
Chemical Property:
  • PSA:0.00000 
  • LogP:2.46040 
Purity/Quality:

98%min *data from raw suppliers

2-CHLORO-1-ETHYNYL-4-FLUOROBENZENE 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of Benzene, 2-chloro-1-ethynyl-4-fluoro-

There total 1 articles about Benzene, 2-chloro-1-ethynyl-4-fluoro- 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 potassium carbonate; In methanol; at 20 ℃; for 16h;
Guidance literature:
With copper(ll) sulfate pentahydrate; sodium L-ascorbate; In water; tert-butyl alcohol; at 20 ℃; regioselective reaction;
DOI:10.1016/j.bmcl.2016.04.015
Guidance literature:
With copper(ll) sulfate pentahydrate; sodium L-ascorbate; In water; tert-butyl alcohol; at 20 ℃; regioselective reaction;
DOI:10.1016/j.bmcl.2016.04.015
Refernces Edit
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