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2-(2-(Bromomethyl)-4-chlorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a chemical compound that serves as a boronic ester reagent in organic synthesis. It is characterized by the presence of a boron atom and is widely recognized for its role in Suzuki-Miyaura cross-coupling reactions, which are pivotal for forming carbon-carbon bonds in organic chemistry. 2-(2-(Bromomethyl)-4-chlorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a versatile and valuable tool for the creation of complex organic molecules, with a broad spectrum of applications across pharmaceutical, agrochemical, and material science research. Its distinctive structure and reactivity position it as a significant building block in the synthesis of a variety of biologically active compounds.

957034-64-9

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957034-64-9 Usage

Uses

Used in Pharmaceutical Research:
2-(2-(Bromomethyl)-4-chlorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is used as a synthetic intermediate for the development of new pharmaceutical compounds. Its unique reactivity allows for the creation of complex molecular structures that can be tailored for specific therapeutic applications, enhancing the discovery and design of novel drugs.
Used in Agrochemical Research:
In the agrochemical industry, 2-(2-(Bromomethyl)-4-chlorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is utilized as a key component in the synthesis of agrochemicals. Its ability to form carbon-carbon bonds is crucial for the development of new pesticides and other agrochemical products that can improve crop protection and yield.
Used in Material Science Research:
2-(2-(Bromomethyl)-4-chlorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is employed as a building block in the synthesis of advanced materials. Its role in creating complex organic molecules contributes to the development of new materials with unique properties for applications in various industries, including electronics, energy, and nanotechnology.
Used in Organic Synthesis:
As a boronic ester reagent, 2-(2-(Bromomethyl)-4-chlorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is used in Suzuki-Miyaura cross-coupling reactions for the formation of carbon-carbon bonds. This application is fundamental in organic synthesis, allowing chemists to construct a wide range of organic compounds with diverse functionalities and structures.

Check Digit Verification of cas no

The CAS Registry Mumber 957034-64-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,7,0,3 and 4 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 957034-64:
(8*9)+(7*5)+(6*7)+(5*0)+(4*3)+(3*4)+(2*6)+(1*4)=189
189 % 10 = 9
So 957034-64-9 is a valid CAS Registry Number.

957034-64-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-(Bromomethyl)-4-chlorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

1.2 Other means of identification

Product number -
Other names 2-[2-(bromomethyl)-4-chlorophenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

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:957034-64-9 SDS

957034-64-9Relevant academic research and scientific papers

OXIDATION RESISTANT INDICATOR MOLECULES

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Page/Page column 79-80, (2008/12/06)

Compounds having enhanced oxidation stability are disclosed. The compounds have an aryl boronic acid residue having one or more electron withdrawing groups on the aromatic moiety which contains the boronic acid residue, such that the molecule has enhanced

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