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5-(N,N-DIMETHYLSULFAMOYL)-2-METHYLPHENYLBORONIC ACID is a boronic acid derivative that is widely utilized in the fields of organic synthesis, pharmaceuticals, and agrochemicals. It is recognized for its selective reactivity with specific functional groups, such as alcohols and amines, and plays a crucial role in Suzuki-Miyaura cross-coupling reactions for the formation of carbon-carbon bonds. 5-(N,N-DIMETHYLSULFAMOYL)-2-METHYLPHENYLBORONIC ACID also finds applications in the development of fluorescent sensors for detecting biological molecules and in the preparation of organoboron compounds for medicinal chemistry research. Furthermore, it has potential applications in materials science, particularly in the development of functionalized polymers and supramolecular materials.

871332-99-9

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871332-99-9 Usage

Uses

Used in Organic Synthesis:
5-(N,N-DIMETHYLSULFAMOYL)-2-METHYLPHENYLBORONIC ACID is used as a reagent for the preparation of various pharmaceuticals and agrochemicals, due to its ability to selectively react with certain functional groups.
Used in Suzuki-Miyaura Cross-Coupling Reactions:
In the field of organic chemistry, 5-(N,N-DIMETHYLSULFAMOYL)-2-METHYLPHENYLBORONIC ACID is used as a coupling agent to form carbon-carbon bonds, which is essential for the synthesis of complex organic molecules.
Used in Fluorescent Sensor Development:
5-(N,N-DIMETHYLSULFAMOYL)-2-METHYLPHENYLBORONIC ACID is used as a component in the development of fluorescent sensors for detecting biological molecules, enabling the monitoring and analysis of various biological processes.
Used in Medicinal Chemistry Research:
This boronic acid derivative is used in the preparation of organoboron compounds, which are crucial for advancing research in medicinal chemistry and the discovery of new therapeutic agents.
Used in Materials Science:
5-(N,N-DIMETHYLSULFAMOYL)-2-METHYLPHENYLBORONIC ACID is used as a building block in the development of functionalized polymers and supramolecular materials, contributing to the creation of innovative materials with unique properties for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 871332-99-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,1,3,3 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 871332-99:
(8*8)+(7*7)+(6*1)+(5*3)+(4*3)+(3*2)+(2*9)+(1*9)=179
179 % 10 = 9
So 871332-99-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H14BNO4S/c1-7-4-5-8(6-9(7)10(12)13)16(14,15)11(2)3/h4-6,12-13H,1-3H3

871332-99-9 Well-known Company Product Price

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  • Alfa Aesar

  • (H52996)  5-Dimethylsulfamoyl-2-methylbenzeneboronic acid, 98%   

  • 871332-99-9

  • 250mg

  • 1158.0CNY

  • Detail
  • Alfa Aesar

  • (H52996)  5-Dimethylsulfamoyl-2-methylbenzeneboronic acid, 98%   

  • 871332-99-9

  • 1g

  • 3704.0CNY

  • Detail

871332-99-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-Dimethyl 3-borono-4-methylbenzenesulfonamide

1.2 Other means of identification

Product number -
Other names [5-(dimethylsulfamoyl)-2-methylphenyl]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:871332-99-9 SDS

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