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2-Chlorothiazol-5-ylboronic acid pinacol ester is a boronic acid derivative that features a thiazole ring and a chloro substituent. It is widely recognized for its role as a building block in organic synthesis, particularly within the realms of pharmaceutical and agrochemical development. The pinacol ester group attached to the molecule endows it with enhanced stability and solubility, qualities that render it an exemplary reagent for cross-coupling reactions and other carbon-carbon bond-forming processes. Its potential as a versatile tool in the synthesis of biologically active compounds has garnered significant attention from medicinal chemists. Furthermore, the boronic acid functionality within this molecule facilitates the formation of stable complexes with other molecules, a feature that extends its utility to the development of diagnostic probes and sensors.

889672-72-4

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889672-72-4 Usage

Uses

Used in Pharmaceutical Development:
2-Chlorothiazol-5-ylboronic acid pinacol ester serves as a crucial building block in the synthesis of various pharmaceuticals. Its unique structure and reactivity make it an indispensable component in the creation of new drugs with specific therapeutic targets.
Used in Agrochemical Synthesis:
In the agrochemical industry, 2-chlorothiazol-5-ylboronic acid pinacol ester is utilized for the development of novel compounds designed to protect crops from pests and diseases, thereby enhancing agricultural productivity.
Used in Organic Synthesis:
As a versatile reagent in organic synthesis, 2-chlorothiazol-5-ylboronic acid pinacol ester is employed in cross-coupling reactions and the formation of carbon-carbon bonds, contributing to the synthesis of complex organic molecules.
Used in Diagnostic Probe and Sensor Development:
The boronic acid functionality of 2-chlorothiazol-5-ylboronic acid pinacol ester allows it to form stable complexes with other molecules, making it a valuable component in the development of diagnostic probes and sensors for detecting specific biological or chemical entities.

Check Digit Verification of cas no

The CAS Registry Mumber 889672-72-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,9,6,7 and 2 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 889672-72:
(8*8)+(7*8)+(6*9)+(5*6)+(4*7)+(3*2)+(2*7)+(1*2)=254
254 % 10 = 4
So 889672-72-4 is a valid CAS Registry Number.

889672-72-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,3-thiazole

1.2 Other means of identification

Product number -
Other names 2-CHLOROTHIAZOLE-5-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:889672-72-4 SDS

889672-72-4Upstream product

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