815631-56-2 Usage
Uses
Used in Pharmaceutical Industry:
4-Fluoro-2-methylphenylboronic acid, pinacol ester is used as a synthetic reagent for the creation of complex organic molecules that are vital in the development of new pharmaceutical compounds. Its ability to form carbon-carbon and carbon-heteroatom bonds makes it a valuable asset in the synthesis of drug candidates.
Used in Agrochemical Development:
In the agrochemical sector, 4-Fluoro-2-methylphenylboronic acid, pinacol ester serves as a key intermediate in the synthesis of various agrochemicals, contributing to the development of effective pesticides and other crop protection agents.
Used in Electronic Materials Production:
4-Fluoro-2-methylphenylboronic acid, pinacol ester is utilized as a precursor in the production of electronic materials, where its chemical properties are harnessed to create components for advanced electronic devices.
Safety and Handling:
It is crucial to handle and store 4-Fluoro-2-methylphenylboronic acid, pinacol ester with caution due to its corrosive nature. Ingestion or inhalation of 4-FLUORO-2-METHYLPHENYLBORONIC ACID, PINACOL ESTER can result in harmful effects, necessitating proper safety measures during its use in laboratories and industrial settings.
Check Digit Verification of cas no
The CAS Registry Mumber 815631-56-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,1,5,6,3 and 1 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 815631-56:
(8*8)+(7*1)+(6*5)+(5*6)+(4*3)+(3*1)+(2*5)+(1*6)=162
162 % 10 = 2
So 815631-56-2 is a valid CAS Registry Number.
InChI:InChI=1/C13H18BFO2/c1-9-8-10(15)6-7-11(9)14-16-12(2,3)13(4,5)17-14/h6-8H,1-5H3
815631-56-2Relevant academic research and scientific papers
Undirected ortho-selectivity in C–H borylation of arenes catalyzed by NHC platinum(0) complexes
Rzhevskiy, Sergey A.,Topchiy, Maxim A.,Golenko, Yulia D.,Gribanov, Pavel S.,Sterligov, Grigorii K.,Kirilenko, Nikita Yu.,Ageshina, Alexandra A.,Bermeshev, Maxim V.,Nechaev, Mikhail S.,Asachenko, Andrey F.
, p. 569 - 571 (2020/10/09)
Borylation of arenes with bis(pinacolato)diboron catalyzed by sterically encumbered NHC platinum complexes proceeds predominantly at ortho-position even in the absence of a directing group (o: m: p ratio up to 10: 3: 1). The similar borylation with pinacolborane would proceed less selectively.
Polycyclic α-amino-ε-caprolactams and related compounds
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Page/Page column 43, (2010/02/14)
Disclosed are polycyclic α-amino-ε-caprolactams and related compounds which are useful as synthetic intermediates in the preparation of inhibitors of β-amyloid peptide release and/or its synthesis.
NK1 ANTAGONIST
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Page/Page column 17, (2010/02/09)
The invention is to a compound exhibiting neurokinin inhibitory properties, a pharmaceutical composition comprising same and a method of treatment for neurokinin-meditated conditions.Formula (I)
