6966-09-2 Usage
Uses
Used in Pharmaceutical Industry:
2-(PIPERIDYLMETHYL)-1-CYCLOHEXANONE HYDROCHLORIDE is used as a precursor in the synthesis of various pharmaceuticals and organic compounds. Its role in the creation of new drugs is significant, as it can be manipulated to produce a range of medicinally relevant molecules.
Used in Drug Development:
2-(PIPERIDYLMETHYL)-1-CYCLOHEXANONE HYDROCHLORIDE is utilized in drug development for its potential to contribute to the creation of novel therapeutic agents. Its unique structure allows for the exploration of new chemical pathways and interactions, which can lead to the discovery of innovative treatments.
Used in Research Applications:
In the field of scientific research, 2-(PIPERIDYLMETHYL)-1-CYCLOHEXANONE HYDROCHLORIDE is employed as a research tool to study the properties and interactions of complex organic molecules. Its use in research helps to advance our understanding of chemical compounds and their potential applications in medicine and other fields.
Check Digit Verification of cas no
The CAS Registry Mumber 6966-09-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,6 and 6 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6966-09:
(6*6)+(5*9)+(4*6)+(3*6)+(2*0)+(1*9)=132
132 % 10 = 2
So 6966-09-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H21NO/c14-12-7-3-2-6-11(12)10-13-8-4-1-5-9-13/h11H,1-10H2/p+1/t11-/m1/s1
6966-09-2Relevant academic research and scientific papers
Synthesis and cytotoxic evaluation of some Mannich bases of alicyclic ketones
Dimmock,Chamankhah,Seniuk,Allen,Kao,Halleran
, p. 668 - 671 (2007/10/03)
A number of Mannich bases of alicyclic ketones containing one and two basic centres were prepared in order to evaluate the theory of sequential cytotoxicity and develop structure-activity relationships in these series of compounds. The compounds were evaluated in vitro against murine P388 D1 lymphocytic leukemia cells. The data generated supported the theory of sequential cytotoxicity and in general, compounds containing alicyclic rings of five and six carbon atoms possessed greater activity than the corresponding dodecyl analogues. Those Mannich bases containing dialkylamino groups were associated with greater cytotoxicity than related compounds possessing a basic heterocycle. Calculations of the atomic charges of the enone groups from selected compounds afforded some rationalization for the cytotoxic screening results.
