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Bis(1H-1,2,4-triazol-1-yl)phosphinic acid 2-chlorophenyl ester

Base Information
  • Chemical Name:Bis(1H-1,2,4-triazol-1-yl)phosphinic acid 2-chlorophenyl ester
  • CAS No.:72351-28-1
  • Molecular Formula:C10H8ClN6O2P
  • Molecular Weight:310.639
  • Hs Code.:
  • DSSTox Substance ID:DTXSID60449390
  • Nikkaji Number:J938.232A
  • Wikidata:Q82268835
Bis(1H-1,2,4-triazol-1-yl)phosphinic acid 2-chlorophenyl ester

Synonyms:72351-28-1;AGN-PC-0NDATZ;SCHEMBL24304589;DTXSID60449390;Bis(1H-1,2,4-triazol-1-yl)phosphinic acid 2-chlorophenyl ester

Suppliers and Price of Bis(1H-1,2,4-triazol-1-yl)phosphinic acid 2-chlorophenyl ester
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of Bis(1H-1,2,4-triazol-1-yl)phosphinic acid 2-chlorophenyl ester
Chemical Property:
  • XLogP3:2
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:4
  • Exact Mass:310.0134882
  • Heavy Atom Count:20
  • Complexity:369
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C(=C1)OP(=O)(N2C=NC=N2)N3C=NC=N3)Cl
Technology Process of Bis(1H-1,2,4-triazol-1-yl)phosphinic acid 2-chlorophenyl ester

There total 1 articles about Bis(1H-1,2,4-triazol-1-yl)phosphinic acid 2-chlorophenyl ester 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 triethylamine; In tetrahydrofuran; at 20 ℃; for 0.5h;
DOI:10.1021/jo00324a010
Guidance literature:
Multi-step reaction with 4 steps
1: dioxane / 2 h / 20 °C
2: 1-methylimidazole / dioxane / 3 h / 20 °C
3: benzenesulfonic acid / CHCl3; methanol / 0.25 h / 0 °C
4: 62 percent / 1-(2,4,6-triisopropylbenzenesulfonyl)-3-nitro-1,2,4-triazole / pyridine / 3.5 h / 20 °C
With 1-(2,4,6-triisopropylbenzenesulfonyl)-3-nitro-1,2,4-triazole; benzenesulfonic acid; 1-methyl-1H-imidazole; In 1,4-dioxane; pyridine; methanol; chloroform;
DOI:10.1002/hlca.19820650803
Guidance literature:
Multi-step reaction with 3 steps
2: H2O / pyridine
3: mesitylenesulfonyl-3-nitrotriazolide
With mesitylenesulfonyl-3-nitrotriazolide; water; In pyridine;
DOI:10.1248/cpb.34.2202
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