CAS 13153-01-0
:2-benzoyl-N-phenylhydrazinecarbothioamide
Description:
2-Benzoyl-N-phenylhydrazinecarbothioamide is an organic compound characterized by its hydrazine and thioamide functional groups. It typically appears as a solid and is known for its potential applications in various fields, including pharmaceuticals and agrochemicals. The presence of the benzoyl and phenyl groups contributes to its aromatic nature, which can influence its reactivity and solubility in organic solvents. This compound may exhibit biological activity, making it of interest in medicinal chemistry for the development of new therapeutic agents. Its structure allows for potential interactions with biological targets, and it may participate in various chemical reactions, such as nucleophilic substitutions or condensation reactions. Additionally, the thioamide group can impart unique properties, such as increased acidity compared to typical amides, which can affect its behavior in chemical reactions. Overall, 2-benzoyl-N-phenylhydrazinecarbothioamide is a compound of interest due to its structural features and potential applications in synthetic and medicinal chemistry.
Formula:C14H13N3OS
InChI:InChI=1S/C14H13N3OS/c18-13(11-7-3-1-4-8-11)16-17-14(19)15-12-9-5-2-6-10-12/h1-10H,(H,16,18)(H2,15,17,19)
InChI key:InChIKey=YFIKTVJZVZMIMY-UHFFFAOYSA-N
SMILES:C(NNC(NC1=CC=CC=C1)=S)(=O)C2=CC=CC=C2
Synonyms:- 1-Benzoyl-4-phenylthiosemicarbazide
- 1-Benzamido-3-phenylthiourea
- Semicarbazide, 1-benzoyl-4-phenyl-3-thio-
- NSC 507159
- Benzoic acid, 2-[(phenylamino)thioxomethyl]hydrazide
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Found 2 products.
1-benzoyl-4-phenyl-3-thiosemicarbazide
CAS:<p>1-Benzoyl-4-phenyl-3-thiosemicarbazide is an adsorbent that has been shown to be a bidentate ligand. It is used as a corrosion inhibitor and exhibits potentiodynamic polarization. The adsorption isotherm of 1-benzoyl-4-phenyl-3-thiosemicarbazide has been measured using Langmuir and Freundlich techniques. This compound has been shown to have fluorescent properties. 1-Benzoyl-4-phenyl-3-thiosemicarbazide also reacts with thiocyanates, yielding the reaction product 1,2,4,5,6 - hexahydrobenzothiazole.</p>Purity:Min. 95%
