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5-bromo-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)picolinonitrile is a chemical compound that features a picolinonitrile core with a bromine atom at the 5th position and a boronate ester functionality at the 3rd position. This molecule serves as a versatile building block in organic synthesis, enabling the creation of more complex chemical structures.
Used in Pharmaceutical Industry:
5-bromo-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)picolinonitrile is used as a synthetic intermediate for the development of pharmaceuticals. Its boronate ester group facilitates Suzuki-Miyaura cross-coupling reactions, which are crucial in the synthesis of various drug molecules.
Used in Agrochemical Industry:
In the agrochemical industry, 5-bromo-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)picolinonitrile is utilized as a key component in the synthesis of agrochemicals. The molecule's ability to undergo cross-coupling reactions allows for the creation of new agrochemical compounds with improved properties.
Used in Materials Science:
5-bromo-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)picolinonitrile is employed as a building block in materials science for the synthesis of advanced materials. The bromine atom and boronate ester functionality provide opportunities for further functionalization, enhancing the molecule's utility in creating novel materials with specific properties.
Used in Organic Synthesis:
As a versatile intermediate in organic synthesis, 5-bromo-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)picolinonitrile is used for the construction of complex organic molecules. Its unique structure allows chemists to explore various synthetic routes and reactions, leading to the development of new compounds with potential applications in various fields.

863868-53-5

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863868-53-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 863868-53-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,3,8,6 and 8 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 863868-53:
(8*8)+(7*6)+(6*3)+(5*8)+(4*6)+(3*8)+(2*5)+(1*3)=225
225 % 10 = 5
So 863868-53-5 is a valid CAS Registry Number.

863868-53-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-bromo-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine-2-carbonitrile

1.2 Other means of identification

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

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:863868-53-5 SDS

863868-53-5Downstream Products

863868-53-5Relevant academic research and scientific papers

Process for producing cyano substituted arene boranes and compounds

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Page/Page column 19, (2008/06/13)

A process for producing cyano substituted arene boranes is described. The compounds are useful intermediates to pharmaceutical compounds using the cyano group as a reactant.

Sterically directed functionalization of aromatic C-H bonds: Selective borylation ortho to cyano groups in arenes and heterocycles

Chotana, Ghayoor A.,Rak, Michael A.,Smith, Milton R.

, p. 10539 - 10544 (2007/10/03)

Ir-catalyzed borylations of 4-substituted benzonitriles are described. In contrast to electrophilic aromatic substitutions and directed ortho metalations, C-H activation/borylation enables functionalization at the 2-position, adjacent to the cyano group, when the 4-subsitutent is larger than cyano. When an excess of borane reagent is used, diborylation can be achieved with a single regioisomer being formed in certain cases. Extension of sterically directed borylation to cyano-substituted, five- and six-membered ring heterocycles is also reported.

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