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1-Propyne, 1,3-dibromo-

Base Information
  • Chemical Name:1-Propyne, 1,3-dibromo-
  • CAS No.:627-16-7
  • Molecular Formula:C3H2Br2
  • Molecular Weight:197.857
  • Hs Code.:
  • European Community (EC) Number:855-353-0
  • DSSTox Substance ID:DTXSID90460856
  • Nikkaji Number:J2.949.493B
  • Wikidata:Q82285012
1-Propyne, 1,3-dibromo-

Synonyms:1-Propyne, 1,3-dibromo-;1,3-dibromoprop-1-yne;627-16-7;1,3-dibromopropyne;1,3-dibromo-propyne;SCHEMBL3663135;DTXSID90460856;EN300-7428154

Suppliers and Price of 1-Propyne, 1,3-dibromo-
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 11 raw suppliers
Chemical Property of 1-Propyne, 1,3-dibromo-
Chemical Property:
  • XLogP3:2.1
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:0
  • Exact Mass:197.85028
  • Heavy Atom Count:5
  • Complexity:63.5
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C(C#CBr)Br
Technology Process of 1-Propyne, 1,3-dibromo-

There total 1 articles about 1-Propyne, 1,3-dibromo- 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 phosphorus tribromide; In pyridine; benzene; for 36h; Ambient temperature;
Refernces

Reaction of thiourea and substituted thioureas with 1,3-dibromopropyne

10.1134/S1070363208100228

The study investigates the reaction of thiourea and various substituted thioureas with 1,3-dibromopropyne to synthesize different thiazolidine derivatives. The chemicals involved include thiourea, N-phenylthiourea, N,N'-diphenylthiourea, N-acetylthiourea, and 1,3-dibromopropyne. These reactants are used to produce 4-bromomethylidene-2-imino(phenylimino, acetylimino)-1,3-thiazolidine hydrobromides and 4-bromomethylidene-2-acetylimino-1,3-thiazolidine under different solvents and temperature conditions. The study explores the reaction mechanism, which likely involves the formation of intermediate bromoethynylmethylsulfides that cyclize into the final thiazolidine products. The products' structures are confirmed through elemental analysis and IR, 1H and 13C NMR spectroscopy data.

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