1116681-99-2 Usage
Uses
Used in Organic Synthesis:
2,3-Difluoro-4-methylphenylboronic acid pinacol ester is used as a building block in organic synthesis for the creation of various pharmaceuticals and agrochemicals. Its unique structure and reactivity make it a valuable component in the synthesis of complex organic molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2,3-difluoro-4-methylphenylboronic acid pinacol ester is employed as a key intermediate in the development of new drugs. Its ability to participate in cross-coupling reactions and other transformations allows for the synthesis of biologically active molecules with potential therapeutic applications.
Used in Cross-Coupling Reactions:
2,3-Difluoro-4-methylphenylboronic acid pinacol ester is used as a reactant in cross-coupling reactions, a class of chemical reactions that facilitate the formation of carbon-carbon bonds. Its participation in these reactions contributes to the synthesis of diverse organic compounds with potential applications in various industries.
Used in Suzuki-Miyaura Coupling:
2,3-Difluoro-4-methylphenylboronic acid pinacol ester is also utilized in Suzuki-Miyaura coupling, a type of cross-coupling reaction that involves the formation of carbon-carbon bonds through the reaction of an organoboronic compound with an organohalide or triflate in the presence of a palladium catalyst. The use of 2,3-difluoro-4-methylphenylboronic acid pinacol ester in this reaction allows for the preparation of a wide range of biologically active molecules.
Used in Chemical Research:
2,3-Difluoro-4-methylphenylboronic acid pinacol ester is used as a research tool in chemical research to explore new synthetic pathways, reaction mechanisms, and the development of novel catalysts and reagents. Its unique properties and reactivity make it an interesting subject for scientific investigation and the advancement of chemical knowledge.
Check Digit Verification of cas no
The CAS Registry Mumber 1116681-99-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,1,6,6,8 and 1 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1116681-99:
(9*1)+(8*1)+(7*1)+(6*6)+(5*6)+(4*8)+(3*1)+(2*9)+(1*9)=152
152 % 10 = 2
So 1116681-99-2 is a valid CAS Registry Number.
1116681-99-2Relevant academic research and scientific papers
2-(2-FLUORO-SUBSTITUTED PHENYL)-6-AMINO-5-CHLORO-4-PYRIMIDINECARBOXYLATES AND THEIR USE AS HERBICIDES
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Page/Page column 7, (2009/03/07)
2-(2-Fluoro-substituted phenyl)-6-amino-5-chloro-4-pyrimidine-carboxylic acid and its derivatives are potent herbicides demonstrating a broad spectrum of weed control.
