1030832-75-7 Usage
Description
4-Chloro-2-methylphenylboronic acid pinacol ester is a versatile chemical compound that integrates the characteristics of both boronic acid and pinacol ester. It is recognized for its high reactivity and capability to form stable complexes with other organic molecules, which makes it a valuable reagent in various organic synthesis processes.
Uses
Used in Pharmaceutical Industry:
4-Chloro-2-methylphenylboronic acid pinacol ester is used as a building block for the synthesis of various pharmaceuticals. Its high reactivity and ability to form stable complexes with other organic molecules contribute to the development of new drugs with improved efficacy and safety profiles.
Used in Agrochemical Industry:
In the agrochemical industry, 4-Chloro-2-methylphenylboronic acid pinacol ester is utilized as a key intermediate in the synthesis of agrochemicals. Its versatile nature allows for the creation of new compounds with enhanced pesticidal properties, contributing to more effective crop protection.
Used in Materials Science:
4-Chloro-2-methylphenylboronic acid pinacol ester is employed as a component in the development of new materials. Its reactivity and complex-forming ability enable the synthesis of materials with unique properties, such as improved mechanical strength, thermal stability, or electrical conductivity.
Used in Organic Synthesis:
As a reagent in organic synthesis, 4-Chloro-2-methylphenylboronic acid pinacol ester is used in Suzuki-Miyaura cross-coupling reactions and C-H activation processes. Its high reactivity and ability to form stable complexes facilitate the formation of carbon-carbon bonds, which are crucial for the synthesis of complex organic molecules.
Used in Research and Development:
4-Chloro-2-methylphenylboronic acid pinacol ester is used as a research tool by chemists and researchers in the field of organic chemistry. Its relatively low toxicity and versatile nature make it a popular choice for exploring new reaction pathways and developing innovative synthetic methods.
Check Digit Verification of cas no
The CAS Registry Mumber 1030832-75-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,0,8,3 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1030832-75:
(9*1)+(8*0)+(7*3)+(6*0)+(5*8)+(4*3)+(3*2)+(2*7)+(1*5)=107
107 % 10 = 7
So 1030832-75-7 is a valid CAS Registry Number.
1030832-75-7Relevant articles and documents
Electrochemical Thiolation and Borylation of Arylazo Sulfones with Thiols and B2pin2
Wang, Rongkang,Chen, Fangming,Jiang, Lvqi,Yi, Wenbin
supporting information, p. 1904 - 1911 (2021/02/12)
An efficient electrochemical synthesis approach of various unsymmetrical thioethers and arylboronates has been developed. Bench stable arylazo sulfones were used as radical precursors for carbon-heteroatom bond formation under electrochemical conditions. Moreover, the scalability of this approach was evaluated by performing the electrochemical thiolation and borylation of arylazo sulfones with thiols and B2pin2 on a gram scale. This protocol not only avoided the use of stoichiometric oxidants, metal catalysts, activating agents and even added bases, but also exhibited favorable functional group tolerance. (Figure presented.).
