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5-Formylpyridine-3-boronic acid pinacol ester is a chemical compound that functions as a reagent in organic synthesis, particularly for Suzuki-Miyaura cross-coupling reactions. It is a derivative of 5-formylpyridine, characterized by the presence of a boron atom bonded to the carbon atom of the formyl group. 5-FORMYLPYRIDINE-3-BORONIC ACID PINACOL ESTER is recognized for its utility in creating biologically active molecules and coordination complexes, making it a significant building block in the synthesis of organic compounds. It also contributes to the development of new materials and catalysts.

848093-29-8

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848093-29-8 Usage

Uses

Used in Pharmaceutical Industry:
5-Formylpyridine-3-boronic acid pinacol ester is used as a key intermediate in the synthesis of various biologically active molecules. Its role in creating complex organic compounds is crucial for the development of new pharmaceuticals, enhancing the range of treatments available for various medical conditions.
Used in Agrochemical Industry:
In the agrochemical sector, 5-Formylpyridine-3-boronic acid pinacol ester serves as a vital component in the production of coordination complexes. These complexes are essential for the development of new agrochemicals, which can improve crop protection and yield.
Used in Organic Synthesis:
5-Formylpyridine-3-boronic acid pinacol ester is utilized as a reagent in Suzuki-Miyaura cross-coupling reactions, a widely used method in organic chemistry for the formation of carbon-carbon bonds. This application is fundamental for the creation of a diverse array of organic compounds, including those with potential applications in materials science and catalysis.
Used in the Development of New Materials:
5-FORMYLPYRIDINE-3-BORONIC ACID PINACOL ESTER is employed as a building block in the synthesis of new materials, leveraging its unique structural properties to contribute to the advancement of material science.
Used in Catalyst Development:
5-Formylpyridine-3-boronic acid pinacol ester is also used in the development of catalysts, where its ability to form stable complexes can enhance the efficiency of various chemical reactions, thereby improving industrial processes and outcomes.

Check Digit Verification of cas no

The CAS Registry Mumber 848093-29-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,8,0,9 and 3 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 848093-29:
(8*8)+(7*4)+(6*8)+(5*0)+(4*9)+(3*3)+(2*2)+(1*9)=198
198 % 10 = 8
So 848093-29-8 is a valid CAS Registry Number.
InChI:InChI=1S/C12H16BNO3/c1-11(2)12(3,4)17-13(16-11)10-5-9(8-15)6-14-7-10/h5-8H,1-4H3

848093-29-8 Well-known Company Product Price

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  • Alfa Aesar

  • (H37151)  5-Formylpyridine-3-boronic acid pinacol ester, 97%   

  • 848093-29-8

  • 1g

  • 645.0CNY

  • Detail
  • Alfa Aesar

  • (H37151)  5-Formylpyridine-3-boronic acid pinacol ester, 97%   

  • 848093-29-8

  • 5g

  • 3214.0CNY

  • Detail

848093-29-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinaldehyde

1.2 Other means of identification

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

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:848093-29-8 SDS

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