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5-Chloro-2-(methylsulfonyl)pyrimidine-4-carboxylic acid is a chemical compound that belongs to the group of pyrimidines and their derivatives. It is characterized by the presence of a chlorine atom, a methylsulfonyl group, and a carboxylic acid group attached to the pyrimidine core. 5-CHLORO-2-(METHYLSULFONYL)PYRIMIDINE-4-CARBOXYLIC ACID is utilized in various chemical reactions as an intermediate for the synthesis of more complex chemicals. The physical properties of 5-CHLORO-2-(METHYLSULFONYL)PYRIMIDINE-4-CARBOXYLIC ACID, such as melting point, boiling point, density, solubility, and stability, can vary depending on the conditions it is exposed to. Due to the reactivity of the pyrimidine moiety and the corrosiveness of the carboxylic acid group, appropriate safety measures are necessary during its handling and storage.

38275-34-2

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38275-34-2 Usage

Uses

Used in Chemical Synthesis:
5-CHLORO-2-(METHYLSULFONYL)PYRIMIDINE-4-CARBOXYLIC ACID is used as a chemical intermediate for the synthesis of more complex chemicals. Its unique structure allows it to be a key component in the production of various compounds, contributing to the advancement of the chemical industry.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 5-CHLORO-2-(METHYLSULFONYL)PYRIMIDINE-4-CARBOXYLIC ACID is used as a building block for the development of new drugs. Its chemical properties make it a valuable asset in the creation of potential therapeutic agents, with the aim of improving healthcare and treatment options.
Used in Research and Development:
5-CHLORO-2-(METHYLSULFONYL)PYRIMIDINE-4-CARBOXYLIC ACID is used as a research compound in academic and industrial laboratories. It serves as a subject for studying chemical reactions, mechanisms, and properties, which can lead to a better understanding of pyrimidine chemistry and its applications in various fields.
Used in Material Science:
In the field of material science, 5-CHLORO-2-(METHYLSULFONYL)PYRIMIDINE-4-CARBOXYLIC ACID is used as a component in the development of new materials. Its unique chemical structure can contribute to the creation of materials with specific properties, such as improved stability or reactivity, which can be beneficial in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 38275-34-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,2,7 and 5 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 38275-34:
(7*3)+(6*8)+(5*2)+(4*7)+(3*5)+(2*3)+(1*4)=132
132 % 10 = 2
So 38275-34-2 is a valid CAS Registry Number.

38275-34-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-chloro-2-methylsulfonylpyrimidine-4-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2-methanesulfonyl-5-chloro-4-pyrimidinecarboxylic acid

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:38275-34-2 SDS

38275-34-2Relevant academic research and scientific papers

Efficient synthesis of a new pyrimidine derivative

Liang, Yong-Min,Luo, Sheng-Jun,Zhang, Zhao-Xin,Ma, Yong-Xiang

, p. 153 - 157 (2002)

A ready preparation for a new pyrimidine derivative, 2-aminomethyl-5-chloropyrimidine, from s-methylthiouronium sulphate and mucochloric acid is reported.

CYCLOALKYLAMINO ACID DERIVATIVES

-

Page/Page column 34, (2008/06/13)

The invention relates to compounds of formula I and to pharmaceutically acceptable salts, prodrugs, solvates or hydrates thereof; wherein B, D, E, R1, R2, R3, R4, R5, R8, m, n, p, q, r, s, t and u are as defined herein. This invention also relates to a method of using such compounds in the treatment of hyperproliferative diseases and autoimmune diseases in mammals, especially humans, and to pharmaceutical compositions containing such compounds.

General and facial synthesis of 2-amino-5-halogenpyrimidine-4-carboxylic acids and their derivatives

Blyumin, Evgeniy V.,Neunhoeffer, Hans,Volovenko, Yulian V.

, p. 2231 - 2241 (2008/02/07)

A facile synthetic approach to 2-amino-5-halogen-pyrimidine-4-carboxylic acids from 5-halogen-2-methylsulfonylpyrimidine-4-carboxylic acid by nucleophilic displacement of the methylsulfonyl group with primary and secondary aliphatic amines has been develo

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