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1073339-12-4

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1073339-12-4 Usage

General Description

2-(5-Bromo-2,3-difluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a chemical compound with the molecular formula C13H15BBrF2O2. It is a boronic acid derivative that is commonly used in organic chemistry as a building block for the synthesis of various pharmaceutical and agrochemical compounds. 2-(5-Bromo-2,3-difluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is known for its ability to function as a versatile and reactive intermediate in a variety of chemical reactions, including Suzuki-Miyaura cross-coupling reactions, which are widely used in the production of pharmaceuticals and other organic compounds. Its unique structure and reactivity make it a valuable tool for chemists and researchers working in the field of chemical synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 1073339-12-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,3,3,3 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1073339-12:
(9*1)+(8*0)+(7*7)+(6*3)+(5*3)+(4*3)+(3*9)+(2*1)+(1*2)=134
134 % 10 = 4
So 1073339-12-4 is a valid CAS Registry Number.

1073339-12-4SDS

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-(5-Bromo-2,3-difluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

1.2 Other means of identification

Product number -
Other names 2-(5-bromo-2,3-difluorophenyl)-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:1073339-12-4 SDS

1073339-12-4Relevant articles and documents

A catalytic borylation/dehalogenation route to o -fluoro arylboronates

Jayasundara, Chathurika R. K.,Unold, Jason M.,Oppenheimer, Jossian,Smith, Milton R.,Maleczka, Robert E.

, p. 6072 - 6075 (2014)

A two-step Ir-catalyzed borylation/Pd-catalyzed dehalogenation sequence allows for the net synthesis of fluoroarenes where the boronic ester is ortho to fluorine. Key elements of this approach include the use of a halogen para to the fluorine to block meta Ir-catalyzed borylation and the chemoselective Pd-catalyzed dehalogenation by KF activated polymethylhydrosiloxane (PMHS).

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