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5-Formylbenzo[b]thiophene-2-boronic acid pinacol ester is a boronic acid derivative that features a thiophene ring and a formyl group. It is widely recognized for its role as a reagent in organic synthesis, particularly for the formation of carbon-carbon and carbon-heteroatom bonds. 5-FORMYLBENZO[B]THIOPHENE-2-BORONIC ACID PINACOL ESTER is also celebrated as a versatile building block in medicinal chemistry and drug discovery, offering the potential to create novel chemical structures with promising biological activity. Furthermore, its unique electronic and optical properties have attracted attention for its potential use in organic light-emitting diodes (OLEDs) and other optoelectronic devices.

953410-99-6

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953410-99-6 Usage

Uses

Used in Organic Synthesis:
5-Formylbenzo[b]thiophene-2-boronic acid pinacol ester is utilized as a reagent for the formation of carbon-carbon and carbon-heteroatom bonds, which are crucial for constructing complex organic molecules.
Used in Medicinal Chemistry and Drug Discovery:
In the field of medicinal chemistry, 5-Formylbenzo[b]thiophene-2-boronic acid pinacol ester serves as a versatile building block. It is used to create novel chemical structures with potential biological activity, contributing to the development of new pharmaceuticals.
Used in Optoelectronic Devices:
5-Formylbenzo[b]thiophene-2-boronic acid pinacol ester is also studied for its potential application in organic light-emitting diodes (OLEDs) and other optoelectronic devices. Its unique electronic and optical properties make it a promising candidate for advancing technology in these areas.

Check Digit Verification of cas no

The CAS Registry Mumber 953410-99-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,3,4,1 and 0 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 953410-99:
(8*9)+(7*5)+(6*3)+(5*4)+(4*1)+(3*0)+(2*9)+(1*9)=176
176 % 10 = 6
So 953410-99-6 is a valid CAS Registry Number.

953410-99-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-benzothiophene-5-carbaldehyde

1.2 Other means of identification

Product number -
Other names 5-Formyl-2-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-benzo[b]thiophene

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:953410-99-6 SDS

953410-99-6Relevant academic research and scientific papers

A versatile method for the hydrolysis of gem-dibromomethylarenes bearing carboxylate or boronate group into aldehydes

Augustine, John Kallikat,Naik, Y. Arthoba,Mandal, Ashis Baran,Chowdappa, Nagaraja,Praveen, Vinuthan B.

, p. 688 - 695 (2008/04/12)

Hydrolysis of gem-dibromomethylarenes bearing carboxylate or boronate group to corresponding aldehydes without affecting the ester group was successfully accomplished in high yields by subjecting them to refluxing pyridine. Both aromatic and heteroaromatic substrates gave the corresponding aldehydes in good yields. This method was efficiently adapted for the large scale synthesis of 2d and 2f.

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