100158-68-7 Usage
General Description
(4-METHYL-PIPERAZIN-1-YL)-(S)-PYRROLIDIN-2-YL-METHANONE is a chemical compound composed of a piperazine ring with a methyl group attached, a pyrrolidine ring, and a methanone functional group. It is commonly used in pharmaceutical research and drug development due to its potential therapeutic properties. The piperazine and pyrrolidine rings are important structural components in many biologically active compounds, making this chemical valuable for exploring new drug candidates. Additionally, the presence of the methyl group and the methanone functional group may contribute to its pharmacological effects. Research into the potential uses and properties of this compound is ongoing.
Check Digit Verification of cas no
The CAS Registry Mumber 100158-68-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,1,5 and 8 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 100158-68:
(8*1)+(7*0)+(6*0)+(5*1)+(4*5)+(3*8)+(2*6)+(1*8)=77
77 % 10 = 7
So 100158-68-7 is a valid CAS Registry Number.
100158-68-7Relevant articles and documents
N-SULFONYLATED PYRAZOLO[3,4-B]PYRIDIN-6-CARBOXAMIDES AND METHOD OF USE
-
Paragraph 00709, (2017/04/23)
The present invention provides for compounds of formula (I) wherein R1, R2, R3, R4, R5, and R6 have any of the values defined in the specification, and pharmaceutically acceptable salts thereof, that are useful as agents in the treatment of diseases and conditions mediated and modulated by CFTR, including cystic fibrosis, Sj?gren's syndrome, pancreatic insufficiency, chronic obstructive lung disease, and chronic obstructive airway disease. Also provided are pharmaceutical compositions comprised of one or more compounds of formula (I).
Chiral amine catalyzed enantio- and diastereoselective Michael reaction in brine
Singh, Sarbjit,Chimni, Swapandeep Singh
, p. 1068 - 1079 (2012/11/06)
Simple pyrrolidine-based chiral amines were synthesized and used for the Michael addition of different ketones to a variety of nitro-olefins in brine. The effect of different surfactants and acids on the yields and stereochemical outcome of the Michael ad
