870486-41-2 Usage
Uses
Used in Pharmaceutical Industry:
2-Chloro-5-fluorobenzeneboronic acid pinacol ester, 96% is used as a building block for the synthesis of various pharmaceuticals. Its unique structure containing both chlorine and fluorine atoms allows for the creation of a wide range of drug candidates with different properties and therapeutic effects.
Used in Agrochemical Industry:
2-Chloro-5-fluorobenzeneboronic acid pinacol ester, 96% is used as a building block for the synthesis of various agrochemicals. Its unique structure containing both chlorine and fluorine atoms allows for the creation of a wide range of agrochemicals with different properties and applications in agriculture.
Used in Organic Synthesis:
2-Chloro-5-fluorobenzeneboronic acid pinacol ester, 96% is used as a valuable chemical reagent in organic synthesis. Its high purity and stability make it suitable for use in sensitive reactions or processes where purity is crucial. The pinacol ester moiety in the compound also enhances its stability and makes it easier to handle and store.
Check Digit Verification of cas no
The CAS Registry Mumber 870486-41-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,0,4,8 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 870486-41:
(8*8)+(7*7)+(6*0)+(5*4)+(4*8)+(3*6)+(2*4)+(1*1)=192
192 % 10 = 2
So 870486-41-2 is a valid CAS Registry Number.
870486-41-2Relevant articles and documents
Fluorine-controlled C-H borylation of arenes catalyzed by a PSiN-pincer platinum complex
Takaya, Jun,Ito, Shisei,Nomoto, Hironori,Saito, Narumasa,Kirai, Naohiro,Iwasawa, Nobuharu
supporting information, p. 17662 - 17665 (2015/12/18)
An efficient, regioselective synthesis of fluorine-substituted arylboronic esters was achieved through fluorine-controlled C-H borylation of arenes with diboron catalyzed by a PSiN-platinum complex. The promising utility of the PSiN-platinum catalyst and its unique regioselectivity were demonstrated for the first time, which would complement the well-developed Ir-catalyzed C-H borylation.
Dipeptidyl peptidase inhibitors
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Page/Page column 37, (2010/02/14)
Compounds, pharmaceutical compositions, kits and methods are provided for use with DPP-IV and other S9 proteases that comprise a compound of the formula: wherein the substituents are as defined herein.
