CAS 5351-69-9: 4-Phenylthiosemicarbazide
Formula:C7H9N3S
InChI:InChI=1S/C7H9N3S/c8-10-7(11)9-6-4-2-1-3-5-6/h1-5H,8H2,(H2,9,10,11)
InChI key:InChIKey=KKIGUVBJOHCXSP-UHFFFAOYSA-N
SMILES:N(C(NN)=S)C1=CC=CC=C1
Synonyms:- 1-Amino-3-phenylthiourea
- 3-Amino-1-phenylthiourea
- 4-Phenyl-3-thiosemicarbazide
- 4-Phenylhydrazinethiocarbamide
- 4-Phenylthiosemicarbazide
- Ai3-00706
- Hydrazinecarbothioamide, N-phenyl-
- N-Phenylhydrazinecarbothioamide
- N-Phenylthiosemicarbazide
- N<sup>1</sup>-Phenylthiosemicarbazide
- Nsc 58946
- See more synonyms
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Found 5 products.
4-Phenyl-3-thiosemicarbazide
CAS:Formula:C7H9N3SPurity:>98.0%(T)(HPLC)Color and Shape:White to Almost white powder to crystalMolecular weight:167.23N-Phenylhydrazinecarbothioamide
CAS:N-Phenylhydrazinecarbothioamide is a chemical compound that is used in wastewater treatment. It is an organic molecule that is composed of hydrophobic and hydrophilic parts. The hydrophobic part, which contains the phenyl group, binds to the hydrophobic region of the cell membrane and causes the cell to lyse. The hydrophilic part has an affinity for water and can be used as an electrode material in electrochemical impedance spectroscopy. N-Phenylhydrazinecarbothioamide also has been shown to have antibacterial properties against human pathogens, including Mycobacterium tuberculosis, Clostridium perfringens, and Escherichia coli O157:H7. The compound has been shown to inhibit cervical cancer cells by inhibiting protein synthesis through inhibition of ribosomal activity and fragmentation assay analysis showed that N-phenylhydrazinecarbothioamide binds to copper ions at a coordination geometry ofFormula:C7H9N3SPurity:Min. 95%Color and Shape:SolidMolecular weight:167.23 g/mol4-Phenylthiosemicarbazide
CAS:Purity:98.0%Color and Shape:Solid, Beige crystallineMolecular weight:167.22999572753906N-Phenylhydrazinecarbothioamide
CAS:Formula:C7H9N3SPurity:98%Color and Shape:SolidMolecular weight:167.2315
