1256358-93-6 Usage
Description
5-Methylindole-2-boronic acid pinacol ester is an organic compound that serves as an intermediate in the synthesis of various organic molecules, particularly in the field of organic chemistry and pharmaceuticals. It is characterized by its unique chemical structure, which includes a boronic acid group and a pinacol ester group, making it a versatile building block for the creation of complex organic compounds.
Uses
Used in Organic Synthesis:
5-Methylindole-2-boronic acid pinacol ester is used as a reactant for the synthesis of azahelicenes and azaheptacirculenes. These compounds are of interest in the field of organic chemistry due to their unique properties and potential applications in various industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 5-Methylindole-2-boronic acid pinacol ester is used as a key intermediate in the development of new drugs. Its unique chemical structure allows for the creation of novel compounds with potential therapeutic applications, making it a valuable tool in the ongoing search for new medications to treat various diseases and conditions.
Used in Chemical Research:
5-Methylindole-2-boronic acid pinacol ester is also utilized in chemical research, where it can be employed to study the properties and reactivity of boronic acid and pinacol ester groups. This can lead to a better understanding of the underlying chemistry and potentially open up new avenues for the development of innovative materials and compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 1256358-93-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,6,3,5 and 8 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1256358-93:
(9*1)+(8*2)+(7*5)+(6*6)+(5*3)+(4*5)+(3*8)+(2*9)+(1*3)=176
176 % 10 = 6
So 1256358-93-6 is a valid CAS Registry Number.
1256358-93-6Relevant articles and documents
Iridium(I)-Catalyzed C?H Borylation in Air by Using Mechanochemistry
Pang, Yadong,Ishiyama, Tatsuo,Kubota, Koji,Ito, Hajime
supporting information, p. 4654 - 4659 (2019/03/17)
Mechanochemistry has been applied for the first time to an iridium(I)-catalyzed C?H borylation reaction. By using either none or just a catalytic amount of a liquid, the mechanochemical C?H borylation of a series of heteroaromatic compounds proceeded in air to afford the corresponding arylboronates in good-to-excellent yields. A one-pot mechanochemical C?H borylation/Suzuki–Miyaura cross-coupling sequence for the direct synthesis of 2-aryl indole derivatives is also described. The present study constitutes an important milestone towards the development of industrially attractive solvent-free C?H bond functionalization processes in air.
