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6-Mercapto-4(1H)-pyrimidinone is an organic compound characterized by its molecular formula C4H4N2OS. It is a pyrimidinone derivative featuring a thiol group (–SH) at the 6th carbon atom. Known for its diverse chemical properties, 6-Mercapto-4(1H)-pyrimidinone serves as a key building block in the synthesis of pharmaceuticals, agrochemicals, and materials. Its potential as an enzyme inhibitor, along with its anti-cancer and anti-viral properties, underscores its significance in the scientific community. 6-Mercapto-4(1H)-pyrimidinone's heterocyclic structure and capacity to form coordination complexes with metal cations further enhance its value across various chemical applications.

6311-83-7

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6311-83-7 Usage

Uses

Used in Pharmaceutical Industry:
6-Mercapto-4(1H)-pyrimidinone is utilized as a synthetic intermediate for the development of various pharmaceuticals. Its unique structure allows for the creation of new drug candidates with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 6-Mercapto-4(1H)-pyrimidinone is employed as a precursor in the synthesis of agrochemicals, contributing to the development of effective pest control agents and other agricultural products.
Used in Materials Science:
6-Mercapto-4(1H)-pyrimidinone is used as a building block in the synthesis of novel materials with specific properties, such as conductive polymers or materials with unique optical characteristics.
Used as an Enzyme Inhibitor:
6-Mercapto-4(1H)-pyrimidinone is studied for its potential as an enzyme inhibitor, which could have implications in the treatment of various diseases by modulating enzyme activity.
Used in Anti-Cancer Research:
6-Mercapto-4(1H)-pyrimidinone is explored for its anti-cancer properties, with the potential to target and inhibit the growth of cancer cells, offering a new avenue for cancer therapy.
Used in Anti-Viral Applications:
6-Mercapto-4(1H)-pyrimidinone is also considered for its anti-viral potential, suggesting a possible role in the development of treatments for viral infections.
Used in Coordination Chemistry:
Due to its ability to form coordination complexes with metal cations, 6-Mercapto-4(1H)-pyrimidinone is applied in coordination chemistry, which can lead to the discovery of new materials with specialized functions in areas such as catalysis, sensing, and drug delivery.

Check Digit Verification of cas no

The CAS Registry Mumber 6311-83-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,1 and 1 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6311-83:
(6*6)+(5*3)+(4*1)+(3*1)+(2*8)+(1*3)=77
77 % 10 = 7
So 6311-83-7 is a valid CAS Registry Number.
InChI:InChI=1/C4H4N2OS/c7-3-1-4(8)6-2-5-3/h1-2H,(H2,5,6,7,8)

6311-83-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-sulfanyl-1H-pyrimidin-6-one

1.2 Other means of identification

Product number -
Other names 6-thioxo-5,6-dihydro-1H-pyrimidin-4-one

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:6311-83-7 SDS

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