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4-(N,N-DIMETHYLSULPHONAMIDO)BENZENEBORONIC ACID is a boronic acid compound characterized by the presence of a dimethylsulphonamido functional group attached to a benzene ring. It is known for its high reactivity due to the boronic acid group, which readily forms covalent bonds with other organic molecules. 4-(N,N-DIMETHYLSULPHONAMIDO)BENZENEBORONIC ACID plays a significant role in various fields of organic chemistry, including the synthesis of pharmaceuticals, agrochemicals, and materials science.

486422-59-7

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486422-59-7 Usage

Uses

Used in Organic Chemistry:
4-(N,N-DIMETHYLSULPHONAMIDO)BENZENEBORONIC ACID is used as a reagent for Suzuki-Miyaura cross-coupling reactions, a powerful tool for forming carbon-carbon bonds. Its high reactivity and ability to form covalent bonds make it a valuable component in organic synthesis processes.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, 4-(N,N-DIMETHYLSULPHONAMIDO)BENZENEBORONIC ACID is used as a key intermediate in the synthesis of various drug molecules. Its unique structure and reactivity contribute to the development of new pharmaceutical compounds with potential therapeutic applications.
Used in Agrochemical Synthesis:
4-(N,N-DIMETHYLSULPHONAMIDO)BENZENEBORONIC ACID is also utilized in the agrochemical industry for the synthesis of pesticides and other agrochemical products. Its reactivity and functional group allow for the creation of novel compounds with improved efficacy and selectivity in agricultural applications.
Used in Materials Science:
In the field of materials science, 4-(N,N-DIMETHYLSULPHONAMIDO)BENZENEBORONIC ACID is employed in the development of new materials with specific properties. Its ability to form covalent bonds with other molecules enables the creation of materials with tailored characteristics for various applications, such as sensors, catalysts, and advanced materials for energy storage and conversion.

Check Digit Verification of cas no

The CAS Registry Mumber 486422-59-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,6,4,2 and 2 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 486422-59:
(8*4)+(7*8)+(6*6)+(5*4)+(4*2)+(3*2)+(2*5)+(1*9)=177
177 % 10 = 7
So 486422-59-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H12BNO4S/c1-10(2)15(13,14)8-5-3-7(4-6-8)9(11)12/h3-6,11-12H,1-2H3

486422-59-7 Well-known Company Product Price

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  • Alfa Aesar

  • (H52936)  4-(Dimethylsulfamoyl)benzeneboronic acid, 95%   

  • 486422-59-7

  • 250mg

  • 1338.0CNY

  • Detail
  • Alfa Aesar

  • (H52936)  4-(Dimethylsulfamoyl)benzeneboronic acid, 95%   

  • 486422-59-7

  • 1g

  • 4279.0CNY

  • Detail

486422-59-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(N,N-Dimethylsulfamoyl)phenylboronic acid

1.2 Other means of identification

Product number -
Other names [4-(dimethylsulfamoyl)phenyl]boronic 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:486422-59-7 SDS

486422-59-7Relevant articles and documents

HALOALLYLAMINE SULFONE DERIVATIVE INHIBITORS OF LYSYL OXIDASES AND USES THEREOF

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Paragraph 0296, (2020/02/23)

The present invention relates to novel compounds which are capable of inhibiting certain amine oxidase enzymes. These compounds are useful for treatment of a variety of indications, e.g., fibrosis, cancer and/or angiogenesis in human subjects as well as i

New phenylpyridylpiperazine compounds

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Page/Page column 8, (2008/06/13)

A compound selected from those of formula (I): [image] wherein: X represents a C(O) or SO2 group, R1 represents an aryl group or a group NR3R4 wherein R3 and R4 are as defined in the description, R2 represents an alkyl, (C3-C8)cycloalkyl or (C3-C8)cycloalkyl-(C1-C6)alkyl group, its isomers, and addition salts thereof, and medicinal products containing the same which are useful in treating conditions treatable by antagonists of type H3 central histamine receptors.

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