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2-Ethylpyridine-4-boronic acid pinacol ester is a versatile chemical compound that features a boronic acid group and a pinacol ester group. This molecule is known for its reactivity and functionality, provided by the 2-ethylpyridine group, and enhanced stability and solubility due to the pinacol ester group. It serves as a valuable building block in the synthesis of complex organic molecules and is widely recognized for its potential applications across various industries.

741709-60-4

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741709-60-4 Usage

Uses

Used in Pharmaceutical Industry:
2-Ethylpyridine-4-boronic acid pinacol ester is used as a key intermediate in the synthesis of pharmaceuticals for its ability to facilitate the creation of complex organic molecules. Its reactivity and stability make it an ideal candidate for developing new drugs with improved efficacy and safety profiles.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Ethylpyridine-4-boronic acid pinacol ester is utilized as a precursor in the development of new agrochemicals. Its unique structure allows for the synthesis of compounds with targeted biological activity, contributing to the creation of more effective and environmentally friendly pesticides and herbicides.
Used in Materials Science:
2-Ethylpyridine-4-boronic acid pinacol ester is employed as a building block in the synthesis of advanced materials. Its properties enable the development of materials with specific characteristics, such as improved mechanical strength, thermal stability, or electrical conductivity, which are crucial for various applications in materials science.
Used in Organic Synthesis:
As a reagent in organic synthesis, 2-Ethylpyridine-4-boronic acid pinacol ester is used for the formation of carbon-carbon and carbon-heteroatom bonds. Its presence in reactions can lead to the creation of a wide range of organic compounds, making it an essential tool for chemists in academic and industrial research settings.
Overall, 2-Ethylpyridine-4-boronic acid pinacol ester is a multifaceted chemical compound with broad applications in various fields, including pharmaceuticals, agrochemicals, materials science, and organic synthesis, due to its unique structural features and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 741709-60-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,1,7,0 and 9 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 741709-60:
(8*7)+(7*4)+(6*1)+(5*7)+(4*0)+(3*9)+(2*6)+(1*0)=164
164 % 10 = 4
So 741709-60-4 is a valid CAS Registry Number.
InChI:InChI=1S/C13H20BNO2/c1-6-11-9-10(7-8-15-11)14-16-12(2,3)13(4,5)17-14/h7-9H,6H2,1-5H3

741709-60-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Ethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

1.2 Other means of identification

Product number -
Other names 2-ethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

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:741709-60-4 SDS

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