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4-(4-Chlorophenyl)pyrimidine-2-thiol, also known as CCPMT, is a pyrimidine derivative with the chemical formula C11H7ClN2S. It features a 4-chlorophenyl substituent and a thiol functional group attached to the 2-position of the pyrimidine ring. 4-(4-Chlorophenyl)pyrimidine-2-thiol has garnered interest due to its potential pharmaceutical applications, including its antimicrobial, antifungal, and anticancer properties, positioning it as a promising candidate for drug development and further research.

175203-08-4

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175203-08-4 Usage

Uses

Used in Pharmaceutical Applications:
4-(4-Chlorophenyl)pyrimidine-2-thiol is used as a potential drug candidate for its antimicrobial, antifungal, and anticancer properties. Its diverse biological activities make it a valuable compound for the development of new therapeutic agents to combat various diseases and infections.
Used in Organic Synthesis:
In the field of organic synthesis, 4-(4-Chlorophenyl)pyrimidine-2-thiol serves as a building block for the preparation of various other compounds. Its unique structure and functional groups allow for the creation of a wide range of chemical entities, expanding the scope of chemical research and innovation.
Used in Antimicrobial Applications:
4-(4-Chlorophenyl)pyrimidine-2-thiol is utilized as an antimicrobial agent, targeting a range of bacteria and helping to combat bacterial infections. Its effectiveness in this area highlights its potential as a component in the development of new antibiotics to address the growing issue of antibiotic resistance.
Used in Antifungal Applications:
4-(4-Chlorophenyl)pyrimidine-2-thiol is also employed as an antifungal agent, effective against various fungi that cause infections in humans and other organisms. Its antifungal properties make it a candidate for the development of new antifungal drugs to treat fungal infections and diseases.
Used in Anticancer Applications:
4-(4-Chlorophenyl)pyrimidine-2-thiol is used as an anticancer agent, showing promise in the fight against cancer. Its potential to target and inhibit the growth of cancer cells positions it as a valuable compound in the ongoing search for new and effective cancer treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 175203-08-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,2,0 and 3 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 175203-08:
(8*1)+(7*7)+(6*5)+(5*2)+(4*0)+(3*3)+(2*0)+(1*8)=114
114 % 10 = 4
So 175203-08-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H7ClN2S/c11-8-3-1-7(2-4-8)9-5-6-12-10(14)13-9/h1-6H,(H,12,13,14)

175203-08-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-(4-chlorophenyl)-1H-pyrimidine-2-thione

1.2 Other means of identification

Product number -
Other names -

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:175203-08-4 SDS

175203-08-4Relevant academic research and scientific papers

Anilinopyrimidine derivatives as IKK inhibitors and compositions and methods related thereto

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, (2008/06/13)

Compounds having activity as inhibitors of IKK are disclosed, particularly IKK-2. The compounds of this invention are anilinopyrimidine derivatives having the following structure: wherein R1 and R6 are as defined herein. Such compounds have utility in the treatment of a wide range of conditions that are responsive to IKK inhibition. Thus, methods of treating such conditions are also disclosed, as are pharmaceutical compositions containing one or more compounds of the above compounds.

Anilinopyrimidine derivatives as JNK pathway inhibitors and compositions and methods related thereto

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, (2008/06/13)

Compounds having activity as inhibitors of the JNK pathway are disclosed. The compounds of this invention are anilinopyrimidine derivatives having the following structure: wherein R1 through R6 are as defined herein. Such compounds have utility in the treatment of a wide range of conditions that are responsive to inhibition of the JNK pathway. Thus, methods of treating such conditions are also disclosed, as are pharmaceutical compositions containing one or more compounds of the above compounds.

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