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Benzo[b]thiophen-4-ylboronic acid pinacol ester is a versatile chemical compound that serves as a building block in the synthesis of various organic compounds. It features a boronic acid functional group attached to a benzo[b]thiophene ring, with a pinacol ester group that enhances stability and solubility. This unique structure and reactivity make it a valuable tool for chemists in the development of new compounds and materials.

1000160-75-7

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1000160-75-7 Usage

Uses

Used in Pharmaceutical Industry:
Benzo[b]thiophen-4-ylboronic acid pinacol ester is used as a synthetic intermediate for the development of pharmaceutical compounds. Its reactivity in Suzuki-Miyaura cross-coupling reactions allows for the formation of C-C bonds, facilitating the synthesis of complex organic molecules with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, Benzo[b]thiophen-4-ylboronic acid pinacol ester is utilized as a precursor in the synthesis of agrochemicals. Its ability to form C-C bonds through cross-coupling reactions enables the creation of novel compounds with potential applications in crop protection and pest control.
Used in Materials Science:
Benzo[b]thiophen-4-ylboronic acid pinacol ester is used as a key component in the synthesis of organic semiconductors and polymers. Its unique structure and reactivity contribute to the development of advanced materials with improved electronic properties, such as organic light-emitting diodes (OLEDs), organic field-effect transistors (OFETs), and organic photovoltaics (OPVs).
Overall, Benzo[b]thiophen-4-ylboronic acid pinacol ester is a multifaceted chemical compound with applications spanning across various industries, including pharmaceuticals, agrochemicals, and materials science. Its role in the synthesis of organic compounds and materials highlights its importance in the development of innovative products and technologies.

Check Digit Verification of cas no

The CAS Registry Mumber 1000160-75-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,0,1,6 and 0 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1000160-75:
(9*1)+(8*0)+(7*0)+(6*0)+(5*1)+(4*6)+(3*0)+(2*7)+(1*5)=57
57 % 10 = 7
So 1000160-75-7 is a valid CAS Registry Number.

1000160-75-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(1-benzothiophen-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

1.2 Other means of identification

Product number -
Other names BENZOTHIOPHENE-4-BORONIC ACID PINACOL ESTER

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:1000160-75-7 SDS

1000160-75-7Upstream product

1000160-75-7Downstream Products

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