1015484-22-6 Usage
General Description
Potassium 1-methyl-4-trifluoroboratomethylpiperazine is a chemical compound that contains potassium, methyl, trifluoroboratomethyl, and piperazine groups. It is commonly used in organic synthesis and pharmaceutical research, and is known for its potential as an active ingredient in drugs targeting neurological disorders. The compound has been studied for its potential as a treatment for conditions such as depression, anxiety, and schizophrenia. Its unique chemical structure and properties make it a valuable component in the development of new pharmaceutical products, and it continues to be an area of interest for researchers and scientists in the field of medicinal chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 1015484-22-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,5,4,8 and 4 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1015484-22:
(9*1)+(8*0)+(7*1)+(6*5)+(5*4)+(4*8)+(3*4)+(2*2)+(1*2)=116
116 % 10 = 6
So 1015484-22-6 is a valid CAS Registry Number.
1015484-22-6Relevant articles and documents
Total synthesis of resorcinol amide Hsp90 inhibitor AT13387
Patel, Bhavesh H.,Barrett, Anthony G. M.
, p. 11296 - 11301 (2012)
The synthesis of C-5-substituted resorcinol amide AT13387, a known Hsp90 inhibitor currently in clinical trials, is reported without the use of phenolic protection in an overall yield of 13.4%. Biomimetic aromatization and Suzuki-Miyaura cross coupling ap
Scope of aminomethylations via Suzuki-Miyaura cross-coupling of orsanotrifluoroborates
Molander, Gary A.,Gormisky, Paul E.,Sandrock, Deidre L.
, p. 2052 - 2057 (2008/09/19)
(Chemical Equation Presented) We previously reported the Suzuki-Miyaura reaction of N,N-dialkylaminomethyltrifluoroborates with aryl bromides. Herein, we report a further investigation of the scope and limitations of this palladium-catalyzed aminomethylation reaction. Aryl chlorides, iodides, and triflates coupled in good to excellent yields to give N,N-dialkylbenzylic amines. The aminomethylation of alkenyl bromides was also examined.
