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4-CHLORO-3-(N-BUTYLAMINOCARBONYL)PHENYLBORONIC ACID is a chemical compound characterized by a boronic acid group attached to a phenyl ring, featuring a butylamino carbonyl group at the 3-position and a chlorine atom at the 4-position. 4-CHLORO-3-(N-BUTYLAMINOCARBONYL)PHENYLBORONIC ACID is recognized for its role in organic synthesis, especially in the creation of carbon-carbon and carbon-nitrogen bonds. Its capacity to form stable complexes with various metal ions renders it a valuable catalyst or ligand in transition metal-catalyzed coupling reactions. The unique structure and reactivity of 4-CHLORO-3-(N-BUTYLAMINOCARBONYL)PHENYLBORONIC ACID establish it as a versatile and significant component in the fields of organic and medicinal chemistry.

871332-94-4

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871332-94-4 Usage

Uses

Used in Organic Synthesis:
4-CHLORO-3-(N-BUTYLAMINOCARBONYL)PHENYLBORONIC ACID is used as a reagent for the formation of carbon-carbon and carbon-nitrogen bonds, which are fundamental in constructing complex organic molecules and pharmaceutical compounds.
Used in Medicinal and Pharmaceutical Research:
In the pharmaceutical industry, 4-CHLORO-3-(N-BUTYLAMINOCARBONYL)PHENYLBORONIC ACID is utilized as a catalyst or ligand in transition metal-catalyzed coupling reactions. Its ability to form stable complexes with metal ions is crucial for the development of new drugs and the improvement of existing ones.
Used in Catalyst and Ligand Development:
4-CHLORO-3-(N-BUTYLAMINOCARBONYL)PHENYLBORONIC ACID is employed in the development of catalysts and ligands for various chemical reactions. Its unique structure allows for fine-tuning of reaction conditions and selectivity, which is essential for the synthesis of specific target molecules in organic chemistry.
Used in Chemical Research:
In the realm of chemical research, 4-CHLORO-3-(N-BUTYLAMINOCARBONYL)PHENYLBORONIC ACID serves as a valuable tool for studying reaction mechanisms and exploring new synthetic pathways. Its versatility in forming complexes and participating in various types of chemical reactions makes it an important subject of investigation for chemists.

Check Digit Verification of cas no

The CAS Registry Mumber 871332-94-4 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 4 respectively.
Calculate Digit Verification of CAS Registry Number 871332-94:
(8*8)+(7*7)+(6*1)+(5*3)+(4*3)+(3*2)+(2*9)+(1*4)=174
174 % 10 = 4
So 871332-94-4 is a valid CAS Registry Number.

871332-94-4 Well-known Company Product Price

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  • Alfa Aesar

  • (H52967)  4-Chloro-3-(n-butylcarbamoyl)benzeneboronic acid, 98%   

  • 871332-94-4

  • 250mg

  • 1158.0CNY

  • Detail

  • Alfa Aesar

  • (H52967)  4-Chloro-3-(n-butylcarbamoyl)benzeneboronic acid, 98%   

  • 871332-94-4

  • 1g

  • 3704.0CNY

  • Detail

871332-94-4SDS

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 (3-(Butylcarbamoyl)-4-chlorophenyl)boronic acid

1.2 Other means of identification

Product number -
Other names [3-(butylcarbamoyl)-4-chlorophenyl]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:871332-94-4 SDS

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