CAS 39136-63-5
:5-Phenyl-2-thiazolamine
Description:
5-Phenyl-2-thiazolamine is an organic compound characterized by its thiazole ring, which is a five-membered heterocyclic structure containing both sulfur and nitrogen atoms. This compound features a phenyl group attached to the thiazole, contributing to its aromatic properties. It is typically a solid at room temperature and may exhibit moderate solubility in polar organic solvents. The presence of the amino group (-NH2) in the thiazole structure allows for potential reactivity, including participation in various chemical reactions such as nucleophilic substitutions and coupling reactions. 5-Phenyl-2-thiazolamine may be of interest in pharmaceutical research due to its potential biological activities, including antimicrobial or anticancer properties. As with many thiazole derivatives, it may also serve as a building block in the synthesis of more complex molecules. Safety data should be consulted for handling and usage, as with any chemical substance, to ensure proper precautions are taken.
Formula:C9H8N2S
InChI:InChI=1S/C9H8N2S/c10-9-11-6-8(12-9)7-4-2-1-3-5-7/h1-6H,(H2,10,11)
InChI key:InChIKey=LSLUWQIENURREM-UHFFFAOYSA-N
SMILES:NC=1SC(=CN1)C2=CC=CC=C2
Synonyms:- 2-Amino-5-phenyl-1,3-thiazole
- 2-Amino-5-phenylthiazol
- 2-Amino-5-phenylthiazole
- 2-Thiazolamine, 5-phenyl-
- 5-Phenyl-1,3-Thiazol-2-Amine
- 5-Phenyl-2-aminothiazole
- 5-Phenyl-2-thiazolamine
- 5-Phenyl-Thiazol-2-Ylamine
- Thiazole, 2-amino-5-phenyl-
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Found 5 products.
5-Phenyl-1,3-thiazol-2-amine
CAS:<p>5-Phenyl-1,3-thiazol-2-amine</p>Purity:97%Color and Shape:SolidMolecular weight:176.23822g/mol5-Phenylthiazol-2-amine
CAS:Formula:C9H8N2SPurity:>98.0%(T)(HPLC)Color and Shape:White to Light yellow powder to crystalMolecular weight:176.245-Phenylthiazol-2-amine
CAS:<p>5-Phenylthiazol-2-amine is a chemical compound with clinical use in the synthesis of dyestuffs and as an intermediate for pharmaceuticals. It is also used for the treatment of cancer, although its clinical efficacy has not been proven. The cellular process that 5-phenylthiazol-2-amine inhibits is the shikimate pathway, which is involved in bacterial metabolism. This compound also inhibits kinases and may be used to treat cancer. 5-Phenylthiazol-2-amine can be synthesized from 2-(4'-nitrophenoxy)benzaldehyde or 2-(4'-nitrophenoxy)benzaldehyde chloride. This chemical reacts with ammonia or ammonium chloride to produce 5-(phenylamino)-1,3,4-thiadiazole (5PT). The reaction mechanism involves nucleophilic substitution at the nitro group followed by hydrolysis of the nitro group to form a</p>Formula:C9H8N2SPurity:Min. 95%Molecular weight:176.24 g/mol




