916791-20-3 Usage
Uses
Used in Pharmaceutical Industry:
[1-(4-TrifluoroMethyl-pyriMidin-2-yl)-piperidin-3-yl]-Methanol, 98+% C11H14F3N3O, MW: 261.24 is used as a potential pharmaceutical intermediate for the development of new drugs, given its unique molecular structure and the presence of the piperidine ring, which is common in many bioactive compounds.
Used in Chemical Research:
In the field of chemical research, [1-(4-TrifluoroMethyl-pyriMidin-2-yl)-piperidin-3-yl]-Methanol, 98+% C11H14F3N3O, MW: 261.24 serves as a valuable compound for studying the effects of trifluoromethyl substitution on the properties and reactivity of organic molecules, as well as for exploring novel synthetic pathways and methodologies.
Used in Material Science:
[1-(4-TrifluoroMethyl-pyriMidin-2-yl)-piperidin-3-yl]-Methanol, 98+% C11H14F3N3O, MW: 261.24 may also find applications in material science, potentially contributing to the development of new materials with unique properties, such as improved stability or specific interactions with biological targets, due to its distinct molecular architecture.
Check Digit Verification of cas no
The CAS Registry Mumber 916791-20-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,6,7,9 and 1 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 916791-20:
(8*9)+(7*1)+(6*6)+(5*7)+(4*9)+(3*1)+(2*2)+(1*0)=193
193 % 10 = 3
So 916791-20-3 is a valid CAS Registry Number.
916791-20-3Relevant academic research and scientific papers
Harnessing Alkylpyridinium Salts as Electrophiles in Deaminative Alkyl-Alkyl Cross-Couplings
Plunkett, Shane,Basch, Corey H.,Santana, Samantha O.,Watson, Mary P.
, p. 2257 - 2262 (2019/03/04)
A Negishi cross-coupling of alkylpyridinium salts and alkylzinc halides has been developed. This is the first example of alkyl-alkyl bond formation via cross-coupling of an alkyl amine derivative with an unactivated alkyl group, and allows both primary and secondary alkylpyridinium salts to react with primary alkylzinc halides with high functional group tolerance. When combined with formation of the pyridinium salts from primary amines, this method enables the noncanonical transformation of NH2 groups into a wide range of alkyl substituents with broad functional group tolerance.
