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2,5-Difluoro-6-methylbenzeneboronic acid, pinacol ester is a boronic acid derivative with the molecular formula C14H17BF2O2 and a molecular weight of 261.097 g/mol. It is a chemical compound commonly used in organic synthesis and medicinal chemistry, featuring a pinacol group, which consists of two hydroxyl groups attached to a central carbon atom. 2,5-Difluoro-6-methylbenzeneboronic acid, pinacol ester serves as a versatile building block in the synthesis of pharmaceuticals, agrochemicals, and new materials, as well as a ligand in transition metal-catalyzed cross-coupling reactions, highlighting its significance in the field of organic chemistry.

1025707-98-5

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1025707-98-5 Usage

Uses

Used in Pharmaceutical Industry:
2,5-Difluoro-6-methylbenzeneboronic acid, pinacol ester is used as a building block for the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents. Its unique structure and reactivity make it a valuable component in the creation of diverse medicinal compounds.
Used in Agrochemical Industry:
In the agrochemical industry, 2,5-Difluoro-6-methylbenzeneboronic acid, pinacol ester is utilized as a key intermediate in the synthesis of agrochemicals, such as pesticides and herbicides. Its incorporation into these products enhances their effectiveness and selectivity in controlling pests and weeds.
Used in Material Science:
2,5-Difluoro-6-methylbenzeneboronic acid, pinacol ester is employed as a component in the development of new materials, including polymers, coatings, and composites. Its unique properties and reactivity contribute to the creation of materials with improved performance characteristics, such as enhanced stability, durability, and functionality.
Used as a Ligand in Organic Chemistry:
In the realm of organic chemistry, 2,5-Difluoro-6-methylbenzeneboronic acid, pinacol ester is used as a ligand in transition metal-catalyzed cross-coupling reactions. Its presence in these reactions facilitates the formation of new carbon-carbon and carbon-heteroatom bonds, enabling the synthesis of complex organic molecules with potential applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 1025707-98-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,5,7,0 and 7 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1025707-98:
(9*1)+(8*0)+(7*2)+(6*5)+(5*7)+(4*0)+(3*7)+(2*9)+(1*8)=135
135 % 10 = 5
So 1025707-98-5 is a valid CAS Registry Number.

1025707-98-5SDS

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 2-(3,6-difluoro-2-methylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

1.2 Other means of identification

Product number -
Other names C-1921

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:1025707-98-5 SDS

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