N-(5-Phenyl-1,2,4-thiadiazol-3-yl)urea

Base Information

Chemical Name:N-(5-Phenyl-1,2,4-thiadiazol-3-yl)urea
CAS No.:89880-03-5
Molecular Formula:C₉H₈N₄OS
Molecular Weight:220.255
Hs Code.:
DSSTox Substance ID:DTXSID70520846
Wikidata:Q82384983

Synonyms:89880-03-5;N-(5-Phenyl-1,2,4-thiadiazol-3-yl)urea;SCHEMBL7656935;DTXSID70520846

Suppliers and Price of N-(5-Phenyl-1,2,4-thiadiazol-3-yl)urea

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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 N-(5-Phenyl-1,2,4-thiadiazol-3-yl)urea

Chemical Property:

XLogP3:1.4
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:220.04188206
Heavy Atom Count:15
Complexity:232

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2=NC(=NS2)NC(=O)N

Technology Process of N-(5-Phenyl-1,2,4-thiadiazol-3-yl)urea

There total 5 articles about N-(5-Phenyl-1,2,4-thiadiazol-3-yl)urea 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: 68.0%

: 97149-60-5
5-phenyl-3-thioureido-1,2,4-thiadiazole

: 89880-03-5
N-(5-phenyl-1,2,4-thiadiazol-3-yl)urea

Guidance literature:: With sodium hydroxide; dihydrogen peroxide; at 75 - 80 ℃; for 0.133333h;

Reference yield: 22.0%

: 89880-02-4
N-carbamoyl-N'-thiobenzoylguanidine

: 27182-54-3
5-phenyl-1,2,4-thiadiazol-3-amine

: 89880-03-5
N-(5-phenyl-1,2,4-thiadiazol-3-yl)urea

Guidance literature:: With di-(p-methoxyphenyl)tellurium oxide; In ethanol; for 1h; Ambient temperature;

Reference yield:

: 7746-72-7
N¹-benzoyl-N³-cyanoguanidine

: 89880-03-5
N-(5-phenyl-1,2,4-thiadiazol-3-yl)urea

Guidance literature:: Multi-step reaction with 2 steps

1: 72 percent / H₂S

2: 22 percent / bis(4-methoxyphenyl)telluroxide / ethanol / 1 h / Ambient temperature

With di-(p-methoxyphenyl)tellurium oxide; hydrogen sulfide; In ethanol;