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54947-91-0

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54947-91-0 Usage

Type of compound

Boronic acid derivative

Usage

Organic synthesis for carbon-carbon and carbon-heteroatom bond formation

Key reaction

Suzuki-Miyaura cross-coupling reactions

Applications

Production of pharmaceuticals, agrochemicals, and materials

Physical state

Water-insoluble, white to off-white crystalline solid

Safety precautions

Potential to cause skin and eye irritation; handle and store with care

Stability

Stable under normal conditions

Decomposition

May occur when exposed to heat, moisture, or incompatible materials

Check Digit Verification of cas no

The CAS Registry Mumber 54947-91-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,9,4 and 7 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 54947-91:
(7*5)+(6*4)+(5*9)+(4*4)+(3*7)+(2*9)+(1*1)=160
160 % 10 = 0
So 54947-91-0 is a valid CAS Registry Number.

54947-91-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-bromophenyl)-1,3,2-dioxaborinane

1.2 Other means of identification

Product number -
Other names 1,3,2-Dioxaborinane,2-(4-bromophenyl)

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:54947-91-0 SDS

54947-91-0Relevant articles and documents

Copper(i)-catalyzed amidation reaction of organoboronic esters and isocyanates

Salim Lew, Tedrick Thomas,Wen Lim, Diane Shu,Zhang, Yugen

supporting information, p. 5140 - 5143 (2015/12/05)

A simple and efficient methodology for the preparation of amides from easily available organoboronic esters and isocyanates has been accomplished using a ligand-free copper(i) catalyst. The reaction system demonstrated a broad substrate scope and provided convenient access to a wide variety of secondary amides.

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