191606-78-7 Usage
Description
1-Methyl-5-(tributylstannyl)-3-(trifluoromethyl)-1H-pyrazole is a complex organic chemical compound characterized by the molecular formula C16H24F3N2Sn. It features a pyrazole ring with a trifluoromethyl group at the 3-position and a tributylstannyl group at the 5-position, attached to different carbon atoms. 1-Methyl-5-(tributylstannyl)-3-(trifluoromethyl)-1H-pyrazole is known for its unique structure and reactivity, which makes it a valuable reagent in organic synthesis and a key intermediate in the production of pharmaceuticals and agrochemicals. However, due to its toxicity and potential health hazards, it must be handled with caution.
Uses
Used in Organic Synthesis:
1-Methyl-5-(tributylstannyl)-3-(trifluoromethyl)-1H-pyrazole is used as a reagent in organic synthesis for its unique reactivity and ability to form various chemical bonds. Its tributylstannyl group can participate in cross-coupling reactions, facilitating the formation of new carbon-carbon or carbon-heteroatom bonds, which are crucial in the synthesis of complex organic molecules.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 1-Methyl-5-(tributylstannyl)-3-(trifluoromethyl)-1H-pyrazole serves as an intermediate in the synthesis of various drugs. Its trifluoromethyl group can impart specific biological activities to the final drug molecules, such as enhancing lipophilicity or modulating metabolic stability, which are essential for drug efficacy and safety.
Used in Agrochemical Production:
Similarly, in the agrochemical sector, 1-Methyl-5-(tributylstannyl)-3-(trifluoromethyl)-1H-pyrazole is utilized as an intermediate for the synthesis of pesticides and other agrochemicals. Its unique structure can contribute to the development of novel agrochemicals with improved performance and selectivity, thus benefiting agricultural productivity and crop protection.
Used in Materials Science:
1-Methyl-5-(tributylstannyl)-3-(trifluoromethyl)-1H-pyrazole also has potential applications in materials science. Its tributylstannyl group can be used to modify the surface properties of materials, such as improving their hydrophobicity or enhancing their adhesion to other materials. Additionally, its trifluoromethyl group can be incorporated into the design of new materials with specific electronic or optical properties, such as organic semiconductors or nonlinear optical materials.
Check Digit Verification of cas no
The CAS Registry Mumber 191606-78-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,1,6,0 and 6 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 191606-78:
(8*1)+(7*9)+(6*1)+(5*6)+(4*0)+(3*6)+(2*7)+(1*8)=147
147 % 10 = 7
So 191606-78-7 is a valid CAS Registry Number.
InChI:InChI=1/C5H4F3N2.3C4H9.Sn/c1-10-3-2-4(9-10)5(6,7)8;3*1-3-4-2;/h2H,1H3;3*1,3-4H2,2H3;/rC17H31F3N2Sn/c1-5-8-11-23(12-9-6-2,13-10-7-3)16-14-15(17(18,19)20)21-22(16)4/h14H,5-13H2,1-4H3
