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25445-02-7

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25445-02-7 Usage

General 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. 5-Phenylthiazole-2-Thiol is commonly used in the synthesis of pharmaceuticals and agrochemicals, and it has also been studied for its potential biological activities, such as antimicrobial and antioxidant properties. 5-Phenylthiazole-2-thiol is a yellow to brown solid with a characteristic odor, and it is soluble in organic solvents such as ethanol and acetone. It is important to handle this chemical with care, as it may be harmful if ingested or inhaled, and it can cause irritation to the skin and eyes.

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)

25445-02-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-phenyl-3H-1,3-thiazole-2-thione

1.2 Other means of identification

Product number -
Other names ZLD0296

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:25445-02-7 SDS

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.

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