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2-Chloro-5-(methylsulfonyl)benzoic acid is a white crystalline solid that belongs to the benzoic acid class. It is an organic intermediate in chemical synthesis, characterized by the presence of a chlorine group and a methylsulfonyl group. These functional groups make it a versatile building block for the development of various chemical compounds and a valuable reagent in organic chemistry for the synthesis of complex molecules and pharmaceuticals.

89938-62-5

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89938-62-5 Usage

Uses

Used in Pharmaceutical Industry:
2-Chloro-5-(methylsulfonyl)benzoic acid is used as an intermediate for the production of pharmaceuticals. Its unique functional groups allow for the synthesis of various drug molecules, contributing to the development of new medications with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 2-chloro-5-(methylsulfonyl)benzoic acid serves as an intermediate for the synthesis of agrochemicals. Its chemical properties enable the creation of compounds that can be used in the development of pesticides, herbicides, and other agricultural chemicals to improve crop protection and yield.
Used in Dye Industry:
2-Chloro-5-(methylsulfonyl)benzoic acid is also utilized as an intermediate in the dye industry. Its chemical structure allows for the synthesis of various dye compounds, which are used in coloring textiles, plastics, and other materials, adding value to these products through coloration and aesthetic enhancement.
Used in Organic Chemistry Research:
As a valuable reagent in organic chemistry, 2-chloro-5-(methylsulfonyl)benzoic acid is employed in the synthesis of complex molecules and pharmaceuticals. Its versatility in chemical reactions makes it an essential component in research laboratories, where it is used to explore new chemical pathways and develop innovative compounds with potential applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 89938-62-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,9,3 and 8 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 89938-62:
(7*8)+(6*9)+(5*9)+(4*3)+(3*8)+(2*6)+(1*2)=205
205 % 10 = 5
So 89938-62-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H7ClO4S/c1-14(12,13)5-2-3-7(9)6(4-5)8(10)11/h2-4H,1H3,(H,10,11)/p-1

89938-62-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-5-methylsulfonylbenzoic acid

1.2 Other means of identification

Product number -
Other names 2-chloro-5-(methylsulfonyl)benzoic 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:89938-62-5 SDS

89938-62-5Relevant academic research and scientific papers

PROTEIN-MACROMOLECULE CONJUGATES AND METHODS OF USE THEREOF

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, (2021/04/10)

The present disclosure provides protein-macromolecule conjugates, releasable linkers, and macromolecules, as defined herein. The disclosed conjugates provide unique properties that are based at least upon the properties of linker and number of linker-Macromolecule moieties. Also provided herein are a method of synthesis and use of conjugates in treating diseases and disorders.

Benzoyl-tetrahydropiperidine derivatives

-

Page/Page column 7, (2008/06/13)

The present invention relates to compounds of formula I wherein R1, R2, and Ar; are as defined in the specification. The invention also provides pharmaceutically acceptable acid addition salts thereof and methods for the treatment of

1- (2-AMINO-BENZOL) -PIPERAZINE DERIVATIVES AS GLYCINE UPTAKE INHIBITORS FOR THE TREATMENT OF PSYCHOSES

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Page/Page column 50, (2008/06/13)

A compound of formula (I) wherein the substituents are described in claim 1 for the treatment of psychoses, pain, neurodegenerative disfunction in memory and learning, schizophrenia, dementia and other diseases in which cognitive processes are impaired, such as attention deficit disorders or Alzheimer's disease.

Method for inhibiting neoplastic cells by exposure to substituted N-cycloalkylmethyl-1-H-pyrazolo (3,4-B) quinolone-4 amines

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, (2008/06/13)

A method for inhibiting neoplastic cells and related conditions by exposing them to substituted N-cycloalkylmethyl-1H-pyrazolo?3,4-b!quinolin-4-amines.

Substituted N-cycloalkylmethyl-1H-pyrazolo(3,4-b)quinolin-4 amines and compositions and methods of use thereof

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, (2008/06/13)

Substituted N-cycloalkylmethyl-1H-pyrazolo[3,4-b]quinolin-4-amines, pharmaceutical compositions containing them and methods for a) effecting c-GMP-phosphodiesterase inhibition, b) treating heart failure and/or hypertension, c) reversing or reducing nitrate-induced tolerance and d) treating angina pectoris, congestive heart disease and myocardial infarction utilizing them.

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