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1-(4-Bromophenyl)-5-mercapto-1,2,3,4-tetrazole

Base Information
  • Chemical Name:1-(4-Bromophenyl)-5-mercapto-1,2,3,4-tetrazole
  • CAS No.:22347-29-1
  • Molecular Formula:C7H5 Br N4 S
  • Molecular Weight:257.113
  • Hs Code.:2933990090
  • DSSTox Substance ID:DTXSID50176880
  • Mol file:22347-29-1.mol
1-(4-Bromophenyl)-5-mercapto-1,2,3,4-tetrazole

Synonyms:1-(4-bromophenyl)-5-mercapto-1,2,3,4-tetrazole;1-BPMT;Br FMT

Suppliers and Price of 1-(4-Bromophenyl)-5-mercapto-1,2,3,4-tetrazole
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
  • AK Scientific
  • 1-(4-Bromophenyl)-5-mercapto-1,2,3,4-tetrazole
  • 5g
  • $ 1718.00
  • AK Scientific
  • 1-(4-Bromophenyl)-5-mercapto-1,2,3,4-tetrazole
  • 1g
  • $ 657.00
  • AK Scientific
  • 1-(4-Bromophenyl)-5-mercapto-1,2,3,4-tetrazole
  • 500mg
  • $ 519.00
Total 4 raw suppliers
Chemical Property of 1-(4-Bromophenyl)-5-mercapto-1,2,3,4-tetrazole
Chemical Property:
  • Vapor Pressure:0.000566mmHg at 25°C 
  • Refractive Index:1.804 
  • Boiling Point:311.4°Cat760mmHg 
  • Flash Point:142.1°C 
  • PSA:82.40000 
  • Density:1.91g/cm3 
  • LogP:1.71350 
  • XLogP3:3.5
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:1
  • Exact Mass:255.94183
  • Heavy Atom Count:13
  • Complexity:237
Purity/Quality:

99% *data from raw suppliers

1-(4-Bromophenyl)-5-mercapto-1,2,3,4-tetrazole *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC(=CC=C1N2C(=S)N=NN2)Br
Technology Process of 1-(4-Bromophenyl)-5-mercapto-1,2,3,4-tetrazole

There total 4 articles about 1-(4-Bromophenyl)-5-mercapto-1,2,3,4-tetrazole 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 sodium azide; for 3h; Heating;
DOI:10.1023/A:1015387108748
Guidance literature:
Multi-step reaction with 2 steps
1: Et3N; EtOCOCl / CHCl3 / -10 - 20 °C
2: aq. NaN3 / 3 h / Heating
With sodium azide; chloroformic acid ethyl ester; triethylamine; In chloroform;
DOI:10.1023/A:1015387108748
Guidance literature:
Multi-step reaction with 3 steps
1: diethyl ether / 2 - 5 °C
2: Et3N; EtOCOCl / CHCl3 / -10 - 20 °C
3: aq. NaN3 / 3 h / Heating
With sodium azide; chloroformic acid ethyl ester; triethylamine; In diethyl ether; chloroform;
DOI:10.1023/A:1015387108748
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