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2-BROMO-3-METHYLPYRIDINE-5-BORONIC ACID PINACOL ESTER is a boronic acid derivative featuring a pyridine ring with a bromine atom at the 2-position and a boronic acid pinacol ester group at the 5-position. It is recognized for its role as a versatile building block in organic synthesis and medicinal chemistry, facilitating the preparation of biologically active molecules and pharmaceuticals. The boronic acid component of 2-BROMO-3-METHYLPYRIDINE-5-BORONIC ACID PINACOL ESTER is particularly notable for its reactivity in Suzuki-Miyaura cross-coupling reactions with aryl halides, thereby enhancing its utility in the synthesis of complex organic compounds. Moreover, the pyridine ring embedded in its structure suggests potential applications in the realms of agrochemicals and materials science, underscoring its value as a synthetic intermediate with a spectrum of chemical applications.

1256360-64-1

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1256360-64-1 Usage

Uses

Used in Organic Synthesis:
2-BROMO-3-METHYLPYRIDINE-5-BORONIC ACID PINACOL ESTER is used as a synthetic intermediate for the creation of complex organic compounds. Its boronic acid functionality allows it to participate in Suzuki-Miyaura cross-coupling reactions, which are crucial for forming carbon-carbon bonds in the assembly of intricate molecular structures.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2-BROMO-3-METHYLPYRIDINE-5-BORONIC ACID PINACOL ESTER is utilized as a building block for the preparation of biologically active molecules. Its structural components can be incorporated into potential drug candidates, contributing to the development of new pharmaceuticals.
Used in Agrochemical Development:
2-BROMO-3-METHYLPYRIDINE-5-BORONIC ACID PINACOL ESTER is used as a chemical component in the development of agrochemicals. The pyridine ring in its structure may offer properties that are beneficial in the design of compounds for agricultural applications, such as pesticides or herbicides.
Used in Materials Science:
Within materials science, 2-BROMO-3-METHYLPYRIDINE-5-BORONIC ACID PINACOL ESTER is employed for its potential to contribute to the development of new materials. The unique structural elements of 2-BROMO-3-METHYLPYRIDINE-5-BORONIC ACID PINACOL ESTER may be harnessed to create materials with specific properties for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1256360-64-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,6,3,6 and 0 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1256360-64:
(9*1)+(8*2)+(7*5)+(6*6)+(5*3)+(4*6)+(3*0)+(2*6)+(1*4)=151
151 % 10 = 1
So 1256360-64-1 is a valid CAS Registry Number.

1256360-64-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Bromo-3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

1.2 Other means of identification

Product number -
Other names 2-bromo-3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

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:1256360-64-1 SDS

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