Thiourea, (5-phenyl-1,2,4-thiadiazol-3-yl)-

Base Information

Chemical Name:Thiourea, (5-phenyl-1,2,4-thiadiazol-3-yl)-
CAS No.:97149-60-5
Molecular Formula:C9H8N4S2
Molecular Weight:236.321
Hs Code.:
DSSTox Substance ID:DTXSID80431595
Nikkaji Number:J1.676.733F
Wikidata:Q82245517

Synonyms:5-phenyl-3-thioureido-1,2,4-thiadiazole;PG301029

Suppliers and Price of Thiourea, (5-phenyl-1,2,4-thiadiazol-3-yl)-

Supply Marketing:

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

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Chemical Property of Thiourea, (5-phenyl-1,2,4-thiadiazol-3-yl)-

Chemical Property:

XLogP3:2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:236.01903862
Heavy Atom Count:15
Complexity:230

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

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

Technology Process of Thiourea, (5-phenyl-1,2,4-thiadiazol-3-yl)-

There total 3 articles about Thiourea, (5-phenyl-1,2,4-thiadiazol-3-yl)- 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: 85.0%

: 97149-59-2
3--5-phenyl-1,2,4-thiadiazole

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

Guidance literature:: With sodium hydroxide; for 0.1h; Heating;

Reference yield: 72.0%

: 123703-07-1
1-ethoxycarbonyl-3-(5'-phenyl-1',2',4'-thiadiazol-3'-yl)thiourea

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

Guidance literature:: With sodium hydroxide; In ethanol; for 1h; Heating;

Reference yield:

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

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

Guidance literature:: Multi-step reaction with 2 steps

1: 82 percent / acetone / 1 h / Heating

2: 85 percent / 3M aq. NaOH / 0.1 h / Heating

With sodium hydroxide; In acetone;