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1,3,2-Dioxaborinane,2,2'-oxybis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

6543-19-7

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6543-19-7 Usage

Usage

Organic synthesis reagent

Specific reactions

Suzuki-Miyaura coupling (carbon-carbon bond formation)

Physical state

Colorless liquid

Boiling point

51-53°C

Flammability

Flammable

Application

Research laboratories and industrial settings

Purpose

Facilitating carbon-carbon bond formation in organic molecules

Safety

Handle with caution and follow safety guidelines

Check Digit Verification of cas no

The CAS Registry Mumber 6543-19-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,4 and 3 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6543-19:
(6*6)+(5*5)+(4*4)+(3*3)+(2*1)+(1*9)=97
97 % 10 = 7
So 6543-19-7 is a valid CAS Registry Number.

6543-19-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name oxybis(1,3,2-dioxaborinane)

1.2 Other means of identification

Product number -
Other names bromo-diphenyl-borane

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:6543-19-7 SDS

6543-19-7Downstream Products

6543-19-7Relevant academic research and scientific papers

Autooxidation of cyclic esters of boric acids

Kuznetsov

, p. 1576 - 1580 (2007/10/03)

1H NMR and IR spectroscopy and mass spectrometry were used to show that the major products of the autooxidation of substituted 1,3,2-dioxaborinanes and 1,3,2-dioxaborolanes upon prolonged handling are the corresponding 2,2′-oxybis(1,3,2-dioxaborinanes) and 2,2′-oxybis(1,3,2-dioxaborolanes). A probable mechanism of this transformation is discussed. 2000 MAIK "Nauka/Interperiodica".

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