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488133-21-7

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488133-21-7 Usage

General Description

2-(4-(Bromomethyl)phenyl)-1,3,2-dioxaborolane is a chemical compound with the molecular formula C8H9BO2Br. It is a boron-containing compound that is often used in organic synthesis as a reagent for Suzuki-Miyaura cross-coupling reactions. 2-(4-(BroMoMethyl)phenyl)-1,3,2-dioxaborolane is a boronic ester, which means it contains a boron atom that is covalently bonded to an oxygen atom and an alkyl or aryl group. The bromomethyl group in its structure makes it reactive and useful for the formation of carbon-carbon bonds in organic molecules. It is also an important building block for the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 488133-21-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,8,1,3 and 3 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 488133-21:
(8*4)+(7*8)+(6*8)+(5*1)+(4*3)+(3*3)+(2*2)+(1*1)=167
167 % 10 = 7
So 488133-21-7 is a valid CAS Registry Number.

488133-21-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[4-(bromomethyl)phenyl]-1,3,2-dioxaborolane

1.2 Other means of identification

Product number -
Other names -

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

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More Details:488133-21-7 SDS

488133-21-7Relevant articles and documents

A synthetic route to 1-(4-boronobenzyl)-1H-pyrrole

D’Silva, Claudius

, p. 655 - 659 (2021)

The synthesis of 1-(4-boronobenzyl)-1H-pyrrole was investigated using three different routes. Two key routes that involved the introduction of the boronate group protected as the pinacol ester, failed, due to deprotection problems. The route involving the

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