[(3-Methylbenzoyl)amino]thiourea

Base Information

Chemical Name:[(3-Methylbenzoyl)amino]thiourea
CAS No.:881-73-2
Molecular Formula:C₉H₁₁N₃OS
Molecular Weight:209.272
Hs Code.:
DSSTox Substance ID:DTXSID101221591

Synonyms:881-73-2;DTXSID101221591;AKOS000295745;3-Methylbenzoic acid 2-(aminothioxomethyl)hydrazide

Suppliers and Price of [(3-Methylbenzoyl)amino]thiourea

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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 [(3-Methylbenzoyl)amino]thiourea

Chemical Property:

XLogP3:1
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:209.06228316
Heavy Atom Count:14
Complexity:232

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=CC(=CC=C1)C(=O)NNC(=S)N

Technology Process of [(3-Methylbenzoyl)amino]thiourea

There total 4 articles about [(3-Methylbenzoyl)amino]thiourea 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: 91.0%

: 13050-47-0
3-methylbenzoyl hydrazine

: 333-20-0
potassium thioacyanate

: 881-73-2
2-(3-methylbenzoyl)hydrazinecarbothioamide

Guidance literature:: With hydrogenchloride;
DOI:10.1016/j.biopha.2017.07.139

Reference yield:

: 79-19-6
thiosemicarbazide

: 1711-06-4
3-Methylbenzoyl chloride

: 881-73-2
2-(3-methylbenzoyl)hydrazinecarbothioamide

Guidance literature:: In tetrahydrofuran; at 0 - 20 ℃; for 24h; Inert atmosphere;
DOI:10.1021/jm400830r

Reference yield:

: 99-36-5
1-methoxycarbonyl-3-methylbenzene

: 881-73-2
2-(3-methylbenzoyl)hydrazinecarbothioamide

Guidance literature:: Multi-step reaction with 2 steps

1: Hydrazine hydrate / ethanol / Heating

2: HCl(conc) / methanol / 4 h / Heating

With hydrogenchloride; hydrazine hydrate; In methanol; ethanol;