N-Benzyl-2-(4-nitrobenzoyl)hydrazinecarbothioamide

Base Information

Chemical Name:N-Benzyl-2-(4-nitrobenzoyl)hydrazinecarbothioamide
CAS No.:282104-46-5
Molecular Formula:C₁₅H₁₄N₄O₃S
Molecular Weight:330.367
Hs Code.:
European Community (EC) Number:657-382-2

Synonyms:N-Benzyl-2-(4-nitrobenzoyl)hydrazinecarbothioamide;AKOS024275458;N-[(BENZYLCARBAMOTHIOYL)AMINO]-4-NITROBENZAMIDE

Suppliers and Price of N-Benzyl-2-(4-nitrobenzoyl)hydrazinecarbothioamide

Supply Marketing:

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

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Chemical Property of N-Benzyl-2-(4-nitrobenzoyl)hydrazinecarbothioamide

Chemical Property:

XLogP3:2.5
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:330.07866149
Heavy Atom Count:23
Complexity:427

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)CNC(=S)NNC(=O)C2=CC=C(C=C2)[N+](=O)[O-]

Technology Process of N-Benzyl-2-(4-nitrobenzoyl)hydrazinecarbothioamide

There total 1 articles about N-Benzyl-2-(4-nitrobenzoyl)hydrazinecarbothioamide 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: 88.0%

: 622-78-6
Benzyl isothiocyanate

: 636-97-5
N-amino-(4-nitrophenyl)carboxamide

: 282104-46-5
4-benzyl-1-(4-nitrobenzoyl)thiosemicarbazide

Guidance literature:: In ethanol; for 6h; Reflux;
DOI:10.1021/acs.jmedchem.9b00912

Reference yield: 78.0%

: 282104-46-5
4-benzyl-1-(4-nitrobenzoyl)thiosemicarbazide

: 23766-17-8
N-benzyl-5-(4-nitrophenyl)-1,3,4-oxadiazole-2-amine

Guidance literature:: With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dimethyl sulfoxide; at 60 ℃; for 2h; regioselective reaction;
DOI:10.1021/jo302324r