536693-96-6 Usage
Uses
Used in Organic Synthesis:
2-Chloro-5-(trifluoromethyl)pyridine-3-boronic acid is used as a building block in the synthesis of other organic molecules. Its boronic acid functionality allows for the formation of carbon-carbon and carbon-oxygen bonds, making it a versatile reagent in organic synthesis.
Used in Pharmaceutical Industry:
2-Chloro-5-(trifluoromethyl)pyridine-3-boronic acid is used as a reagent in coupling reactions for the development of new drugs. Its unique structure and reactivity can be utilized to create novel drug candidates with potential therapeutic applications.
Used in Agrochemical Industry:
2-Chloro-5-(trifluoromethyl)pyridine-3-boronic acid is used as a reagent in the synthesis of agrochemicals. Its ability to form carbon-carbon and carbon-oxygen bonds can contribute to the development of new pesticides, herbicides, or other agricultural chemicals.
Used in Material Science:
2-Chloro-5-(trifluoromethyl)pyridine-3-boronic acid is used as a building block in the development of new materials. Its unique structure and reactivity can be employed to create novel materials with specific properties for various applications in material science.
Check Digit Verification of cas no
The CAS Registry Mumber 536693-96-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,3,6,6,9 and 3 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 536693-96:
(8*5)+(7*3)+(6*6)+(5*6)+(4*9)+(3*3)+(2*9)+(1*6)=196
196 % 10 = 6
So 536693-96-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H4BClF3NO2/c8-5-4(7(13)14)1-3(2-12-5)6(9,10)11/h1-2,13-14H
536693-96-6Relevant articles and documents
Trifluoromethyl-substituted pyridyl- and pyrazolylboronic acids and esters: Synthesis and Suzuki-Miyaura cross-coupling reactions
Clapham, Kate M.,Batsanov, Andrei S.,Bryce, Martin R.,Tarbit, Brian
supporting information; experimental part, p. 2155 - 2161 (2009/09/04)
The synthesis of trifluoromethyl-substituted pyridylboronic acids and pyrazolylboronic esters is described via lithiation-boronation protocols (Schemes 1, 3 and 4). A study of their palladium-catalysed cross-couplings with heteroaryl halides is presented.
DIHYDROXY(3-PYRIDYL)BORANE COMPOUNDS
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Page 6, (2010/02/08)
A dihydroxy(3-pyridyl)borane compound of the formula (1): wherein R1 represents a hydrogen atom, halogen atom or alkoxycarbonylamino group; R2 represents a hydrogen atom, halogen atom, alkyl group or fluoroalkyl group; with the proviso that the case wherein both R1 and R2 are hydrogen atoms is excepted.
