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(6-AMINOPYRIDIN-3-YL)BORONIC ACID, with the molecular formula C5H7BN2O2, is a boronic acid derivative characterized by the presence of a pyridine ring with an amino group at the third carbon and a boronic acid group. (6-AMINOPYRIDIN-3-YL)BORONIC ACID is recognized for its unique reactivity and structural properties, making it a valuable component in various chemical applications.

851524-96-4

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851524-96-4 Usage

Uses

Used in Organic Synthesis:
(6-AMINOPYRIDIN-3-YL)BORONIC ACID is used as a versatile reagent for the Suzuki-Miyaura coupling reaction, a widely employed method in organic synthesis for the formation of carbon-carbon bonds. Its role in this reaction facilitates the creation of new chemical entities with potential applications across different industries.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (6-AMINOPYRIDIN-3-YL)BORONIC ACID is utilized as a ligand for metal-catalyzed cross-coupling reactions. This application is crucial for the development of complex molecular structures found in pharmaceuticals, contributing to the advancement of new drug discoveries.
Used in Pharmaceutical Preparation:
(6-AMINOPYRIDIN-3-YL)BORONIC ACID is used as a key intermediate in the preparation of pharmaceuticals, where its unique chemical properties allow for the synthesis of bioactive compounds with potential therapeutic effects.
Used in Agrochemical Development:
(6-AMINOPYRIDIN-3-YL)BORONIC ACID also finds use in the agrochemical industry, where it is employed in the synthesis of agrochemicals, contributing to the development of new pesticides and other agricultural products to improve crop protection and yield.
Used in Material Science:
(6-AMINOPYRIDIN-3-YL)BORONIC ACID is used in the development of new materials, leveraging its unique reactivity to create advanced materials with specific properties for various applications.
Used in Chemical Sensors:
Due to its structural properties, (6-AMINOPYRIDIN-3-YL)BORONIC ACID has potential applications in the development of chemical sensors, where its reactivity can be harnessed to detect and measure the presence of specific chemical species.

Check Digit Verification of cas no

The CAS Registry Mumber 851524-96-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,1,5,2 and 4 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 851524-96:
(8*8)+(7*5)+(6*1)+(5*5)+(4*2)+(3*4)+(2*9)+(1*6)=174
174 % 10 = 4
So 851524-96-4 is a valid CAS Registry Number.
InChI:InChI=1/C5H7BN2O2/c7-5-2-1-4(3-8-5)6(9)10/h1-3,9-10H,(H2,7,8)

851524-96-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (6-aminopyridin-3-yl)boronic acid

1.2 Other means of identification

Product number -
Other names 5-pyridine-2-amine-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:851524-96-4 SDS

851524-96-4Upstream product

851524-96-4Relevant articles and documents

Process for the preparation of aminoaryl- and aminoheteroaryl boronic acids and esters

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Paragraph 0053; 0056; 0061, (2014/11/27)

The present invention relates to a process for the preparation of aminoaryl- and aminoheteroaryl boronic acids and esters of formula (I) in high yields The claimed process uses diarylketal formula (V) to generate an arylbromid of formula (III) in which the amino-group is protected as bisarylmethylidenimino-group:

PROCESS FOR THE PREPARATION OF AMINOARYL- AND AMINOHETEROARYL BORONIC ACIDS AND ESTERS

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Page/Page column 15; 16; 17; 19, (2014/12/09)

The present invention relates to a process for the preparation of aminoaryl- and aminoheteroaryl boronic acids and esters thereof of formula (I) in high yield. The claimed process uses diarylketal formula (V) to generate an arylbromide of formula (III) in which the amino-group is protected as bisarylmethylidenimino-group, which is then transformed into a formula (I) compound.

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