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138983-68-3

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138983-68-3 Usage

General Description

5-Trimethylsilylthiophene-2-boronic acid is a chemical compound that is used in various organic synthesis reactions as a boronic acid derivative. It features a boronic acid group and a trimethylsilyl group attached to a thiophene ring. 5-TRIMETHYLSILYLTHIOPHENE-2-BORONIC ACID is known for its use in the synthesis of pharmaceuticals, agrochemicals, and materials science. It is a versatile building block for the construction of various organic molecules and is commonly used in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds. Additionally, it can be used in the preparation of functionalized thiophenes and other heterocyclic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 138983-68-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,9,8 and 3 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 138983-68:
(8*1)+(7*3)+(6*8)+(5*9)+(4*8)+(3*3)+(2*6)+(1*8)=183
183 % 10 = 3
So 138983-68-3 is a valid CAS Registry Number.

138983-68-3SDS

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 (5-trimethylsilylthiophen-2-yl)boronic acid

1.2 Other means of identification

Product number -
Other names 5-trimethylsilyl-2-thienylboronic 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:138983-68-3 SDS

138983-68-3Downstream Products

138983-68-3Relevant articles and documents

Novel synthesis of arylboronic acids by electroreduction of aromatic halides in the presence of trialkyl borates

Laza, Carine,Dunach, Elisabet,Serein-Spirau, Francoise,Moreau, Joel J. E.,Vellutini, Luc

, p. 373 - 375 (2002)

A novel preparation of aryl and heteroarylboronic acids by an electrochemical coupling reaction is described. It is based on the reductive coupling between aromatic or heteroaromatic halides and a trialkyl borate. The reactions are carried out in DMF or THF with the use of sacrificial aluminium or magnesium anodes in a single-compartment cell. Arylboronic acids are obtained with moderate to good selectivities and isolated yields.

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