4-Phenyl-1,2,5-thiadiazole-3-carboxamide

Base Information

Chemical Name:4-Phenyl-1,2,5-thiadiazole-3-carboxamide
CAS No.:334709-79-4
Molecular Formula:C₉H₇N₃OS
Molecular Weight:205.24
Hs Code.:
DSSTox Substance ID:DTXSID801273917
Nikkaji Number:J1.501.562D

Synonyms:4-phenyl-1,2,5-thiadiazole-3-carboxamide;SCHEMBL14582775;DTXSID801273917;334709-79-4

Suppliers and Price of 4-Phenyl-1,2,5-thiadiazole-3-carboxamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 4-Phenyl-1,2,5-thiadiazole-3-carboxamide

Chemical Property:

XLogP3:1.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:205.03098303
Heavy Atom Count:14
Complexity:218

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2=NSN=C2C(=O)N

Technology Process of 4-Phenyl-1,2,5-thiadiazole-3-carboxamide

There total 2 articles about 4-Phenyl-1,2,5-thiadiazole-3-carboxamide 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:

Reference yield: 48.0%

: 4369-55-5
3-phenyl-isoxazol-5-ylamine

: 334709-79-4
4-phenyl-1,2,5-thiadiazole-3-carboxamide

Guidance literature:: With tetrasulfur tetranitride antimony(V) chloride; In toluene; at 100 ℃; for 0.5h;

Reference yield:

: 17082-13-2
α-bromoacetophenone oxime

: 334709-79-4
4-phenyl-1,2,5-thiadiazole-3-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: 58 percent / methanol / 0.5 h / 20 °C

2: 48 percent / tetrasulfur tetranitride antimony(V) chloride complex / toluene / 0.5 h / 100 °C

With tetrasulfur tetranitride antimony(V) chloride; In methanol; toluene;