25445-02-7 Usage
Description
5-Phenylthiazole-2-Thiol is a chemical compound with the molecular formula C9H7NS2. It is a thiazole derivative that contains a phenyl group and a thiol group. This yellow to brown solid with a characteristic odor is soluble in organic solvents such as ethanol and acetone. Due to its potential harmful effects if ingested or inhaled, and its ability to cause skin and eye irritation, careful handling is required.
Uses
Used in Pharmaceutical Synthesis:
5-Phenylthiazole-2-Thiol is used as a key intermediate in the synthesis of various pharmaceuticals for its unique chemical properties that contribute to the development of new drugs.
Used in Agrochemical Production:
In the agrochemical industry, 5-Phenylthiazole-2-Thiol is utilized as a building block in the creation of compounds that help protect crops and enhance agricultural productivity.
Used in Antimicrobial Applications:
5-Phenylthiazole-2-Thiol is studied for its potential antimicrobial properties, making it a candidate for use in applications that require the inhibition of microbial growth.
Used in Antioxidant Formulations:
Due to its antioxidant potential, 5-Phenylthiazole-2-Thiol is considered for use in formulations that help prevent oxidative damage in various industrial and biological settings.
Check Digit Verification of cas no
The CAS Registry Mumber 25445-02-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,4,4 and 5 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 25445-02:
(7*2)+(6*5)+(5*4)+(4*4)+(3*5)+(2*0)+(1*2)=97
97 % 10 = 7
So 25445-02-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H7NS2/c11-9-10-6-8(12-9)7-4-2-1-3-5-7/h1-6H,(H,10,11)
25445-02-7Relevant articles and documents
An approach to the synthesis of 4-aryl and 5-aryl substituted thiazole-2(3: H)-thiones employing flow processing
Balti, Monaem,Miller, Shelli A.,Efrit, Mohamed Lotfi,Leadbeater, Nicholas E.
, p. 72165 - 72169 (2016/08/09)
A method for the preparation of 4-aryl and 5-aryl substituted thiazole-2(3H)-thiones is described. Flow processing is employed as a tool, and supported acids and bases used to facilitate both the synthetic strategy and product isolation. The methodology is applicable to a range of substrates.