1030832-71-3 Usage
Description
2-Methyl-5-trifluoroMethylphenylboronic acid, pinacol ester is a boronic acid ester derivative with the molecular formula C14H17BF3O2. It is a white to off-white solid that is commonly used in organic synthesis as a reagent for cross-coupling reactions, particularly in the Suzuki-Miyaura coupling. This chemical compound is often utilized as a building block in the pharmaceutical industry, as well as in the development of agrochemicals and materials science. The pinacol ester form of 2-Methyl-5-trifluoroMethylphenylboronic acid provides certain advantages in terms of stability and solubility, making it a valuable tool in the field of organic chemistry.
Uses
Used in Pharmaceutical Industry:
2-Methyl-5-trifluoroMethylphenylboronic acid, pinacol ester is used as a building block for the synthesis of various pharmaceutical compounds. Its unique structure and reactivity in cross-coupling reactions enable the creation of diverse and complex molecules with potential therapeutic applications.
Used in Agrochemical Development:
In the agrochemical industry, 2-Methyl-5-trifluoroMethylphenylboronic acid, pinacol ester is used as a key intermediate in the synthesis of various agrochemicals. Its versatility in organic synthesis allows for the development of new and effective compounds for crop protection and pest control.
Used in Materials Science:
2-Methyl-5-trifluoroMethylphenylboronic acid, pinacol ester is employed in materials science for the synthesis of novel materials with unique properties. Its ability to participate in cross-coupling reactions facilitates the creation of new materials with potential applications in various fields, such as electronics, energy storage, and advanced materials.
Used in Organic Synthesis:
As a reagent for cross-coupling reactions, particularly in the Suzuki-Miyaura coupling, 2-Methyl-5-trifluoroMethylphenylboronic acid, pinacol ester is used in organic synthesis to form carbon-carbon bonds. This allows for the construction of complex molecular structures and the synthesis of a wide range of organic compounds with various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1030832-71-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,0,8,3 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1030832-71:
(9*1)+(8*0)+(7*3)+(6*0)+(5*8)+(4*3)+(3*2)+(2*7)+(1*1)=103
103 % 10 = 3
So 1030832-71-3 is a valid CAS Registry Number.
1030832-71-3Relevant articles and documents
NOVEL SUBSTITUTED INDOLE DERIVATIVES AS GAMMA SECRETASE MODULATORS
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Page/Page column 75, (2013/03/26)
The present invention is concerned with novel substituted indole derivatives of Formula (I) wherein R1, R2, R3, A1, A2, A3, Y and X have the meaning defined in the claims. The compounds according to the present invention are useful as gamma secretase modulators. The invention further relates to processes for preparing such novel compounds, pharmaceutical compositions comprising said compounds as an active ingredient as well as the use of said compounds as a medicament.
