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3-Boronobenzyl chloride is an organoboron compound with the chemical formula C7H7BCl. It is a colorless liquid that is commonly used as a reagent in organic synthesis.

957035-15-3

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957035-15-3 Usage

Uses

Used in Organic Synthesis:
3-Boronobenzyl chloride is used as a reagent for introducing a boron group into organic compounds, which is crucial for the development of new molecules with potential applications in medicinal and materials chemistry.
Used in Pharmaceutical Synthesis:
3-Boronobenzyl chloride is used as a building block in the synthesis of pharmaceuticals and other biologically active compounds, contributing to the discovery and development of new drugs.
Used in Preparation of Boronate Esters:
3-Boronobenzyl chloride is used in the preparation of boronate esters, which are important intermediates in organic chemistry, facilitating various chemical reactions and transformations.

Check Digit Verification of cas no

The CAS Registry Mumber 957035-15-3 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 5 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 957035-15:
(8*9)+(7*5)+(6*7)+(5*0)+(4*3)+(3*5)+(2*1)+(1*5)=183
183 % 10 = 3
So 957035-15-3 is a valid CAS Registry Number.

957035-15-3SDS

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 [3-(chloromethyl)phenyl]boronic acid

1.2 Other means of identification

Product number -
Other names 3-Chloromethylphenylboronic 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:957035-15-3 SDS

957035-15-3Downstream Products

957035-15-3Relevant academic research and scientific papers

Effective Utilization of Flow Chemistry: Use of Unstable Intermediates, Inhibition of Side Reactions, and Scale-Up for Boronic Acid Synthesis

Usutani, Hirotsugu,Cork, David G.

, p. 741 - 746 (2018)

Flow chemistry processes for boronic acid syntheses utilizing lithiation-borylation have been developed. The side reactions in the lithiation step that occur in batch were suppressed, and unstable lithium intermediates were handled safely. Flow technology was applied to several kinds of boronic acid syntheses, and scale-up was successfully conducted to allow kilogram-scale production. Some of the key benefits of flow flash chemistry were utilized, both to avoid side reactions and to enable dianion chemistry that is difficult to perform successfully in batch reactions. The examples showed further perspectives on the utility of flow technologies for process development.

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