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1,4-diamino-2-butyne

Base Information
  • Chemical Name:1,4-diamino-2-butyne
  • CAS No.:53878-96-9
  • Molecular Formula:C4H8N2
  • Molecular Weight:84.1209
  • Hs Code.:2921290000
  • Mol file:53878-96-9.mol
1,4-diamino-2-butyne

Synonyms:1,4-Diamino-2-butyne;

Suppliers and Price of 1,4-diamino-2-butyne
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 10 raw suppliers
Chemical Property of 1,4-diamino-2-butyne
Chemical Property:
  • Vapor Pressure:0.374mmHg at 25°C 
  • Melting Point:44°C 
  • Refractive Index:1.513 
  • Boiling Point:197.7 °C at 760 mmHg 
  • Flash Point:84.3 °C 
  • PSA:52.04000 
  • Density:0.987 g/cm3 
  • LogP:0.30780 
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • General Description 1,4-Diamino-2-butyne is a versatile compound with notable chemical and physiological properties, serving as a key intermediate in the synthesis of unsymmetrical derivatives through efficient Cu(I)-catalyzed cross-coupling reactions. It can be derived from 1,4-dichloro-2-butyne and forms bis(amino acid) derivatives that adopt a C2-symmetric turn conformation stabilized by intramolecular hydrogen bonds, as demonstrated by NMR studies. These structural features highlight its utility in designing conformationally constrained peptidomimetics and other bioactive molecules.
Technology Process of 1,4-diamino-2-butyne

There total 9 articles about 1,4-diamino-2-butyne 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 ammonium hydroxide; at 40 ℃; for 3h;
DOI:10.1016/S0968-0896(03)00521-2
Guidance literature:
N-methyl-N-allylamine; formaldehyd; In acetonitrile; at 20 ℃;
di-n-propylamine; Propiolic acid; With copper(l) iodide; In acetonitrile; at 80 ℃; for 0.5h; chemoselective reaction; Sealed tube; Microwave irradiation;
DOI:10.1021/acs.joc.1c00537
Guidance literature:
N-methyl-N-allylamine; formaldehyd; In acetonitrile; at 20 ℃;
dibutylamine; Propiolic acid; With copper(l) iodide; In acetonitrile; at 80 ℃; for 0.5h; chemoselective reaction; Sealed tube; Microwave irradiation;
DOI:10.1021/acs.joc.1c00537
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