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2-AMINO-5-(4-AMYLPHENYL)-1,3,4-THIADIAZOLE

Base Information Edit
  • Chemical Name:2-AMINO-5-(4-AMYLPHENYL)-1,3,4-THIADIAZOLE
  • CAS No.:114751-76-7
  • Molecular Formula:C13H17N3S
  • Molecular Weight:247.35900
  • Hs Code.:2934999090
  • Mol file:114751-76-7.mol
2-AMINO-5-(4-AMYLPHENYL)-1,3,4-THIADIAZOLE

Synonyms:

Suppliers and Price of 2-AMINO-5-(4-AMYLPHENYL)-1,3,4-THIADIAZOLE
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
  • TRC
  • 5-(4-Pentyl-phenyl)-[1,3,4]thiadiazol-2-ylamine
  • 50mg
  • $ 110.00
  • Matrix Scientific
  • 5-(4-Pentyl-phenyl)-[1,3,4]thiadiazol-2-ylamine
  • 500mg
  • $ 160.00
  • Crysdot
  • 5-(4-Pentylphenyl)-1,3,4-thiadiazol-2-amine 97%
  • 5g
  • $ 853.00
  • American Custom Chemicals Corporation
  • 5-(4-PENTYL-PHENYL)-[1,3,4]THIADIAZOL-2-YLAMINE 95.00%
  • 500MG
  • $ 795.80
  • AK Scientific
  • 5-(4-Pentyl-phenyl)-[1,3,4]thiadiazol-2-ylamine
  • 500mg
  • $ 266.00
Total 2 raw suppliers
Chemical Property of 2-AMINO-5-(4-AMYLPHENYL)-1,3,4-THIADIAZOLE Edit
Chemical Property:
  • PSA:80.04000 
  • LogP:4.10120 
Purity/Quality:

98%min *data from raw suppliers

5-(4-Pentyl-phenyl)-[1,3,4]thiadiazol-2-ylamine *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of 2-AMINO-5-(4-AMYLPHENYL)-1,3,4-THIADIAZOLE

There total 3 articles about 2-AMINO-5-(4-AMYLPHENYL)-1,3,4-THIADIAZOLE 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 trichlorophosphate; at 0 - 70 ℃; for 4.5h;
DOI:10.3184/174751914X13990224465880
Guidance literature:
With sulfuric acid; at 40 - 50 ℃; Yield given;
Guidance literature:
Multi-step reaction with 2 steps
1: 90 percent / pyridine / Ambient temperature; left overnight
2: conc. H2SO4 / 40 - 50 °C
With pyridine; sulfuric acid;
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