1258639-71-2 Usage
Uses
Used in Pharmaceutical Industry:
C11H21N3O2ClH is used as a pharmaceutical compound for its potential biological activity. The presence of nitrogen in the molecule suggests that it may interact with biological systems, such as proteins or enzymes, and the chloride ion may contribute to its solubility or stability in physiological conditions.
Used in Chemical Research:
C11H21N3O2ClH can be used as a subject of chemical research to explore its properties, reactivity, and potential applications. C11H21N3O2ClH's structure and the role of the chloride ion as a counterion may provide insights into the design of new molecules with specific functions or improved properties.
Used in Material Science:
C11H21N3O2ClH may have potential applications in material science, particularly if its properties can be tailored through chemical modifications or interactions with other molecules. C11H21N3O2ClH could be studied for its potential use in the development of new materials with specific characteristics, such as conductivity, stability, or responsiveness to environmental stimuli.
Check Digit Verification of cas no
The CAS Registry Mumber 1258639-71-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,8,6,3 and 9 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1258639-71:
(9*1)+(8*2)+(7*5)+(6*8)+(5*6)+(4*3)+(3*9)+(2*7)+(1*1)=192
192 % 10 = 2
So 1258639-71-2 is a valid CAS Registry Number.
1258639-71-2Relevant academic research and scientific papers
Young, Robert J.,Alderton, Wendy,Angell, Anthony D.R.,Beswick, Paul J.,Brown, David,Chambers, C. Lynn,Crowe, Miriam C.,Dawson, John,Hamlett, Christopher C.F.,Hodgson, Simon T.,Kleanthous, Savvas,Knowles, Richard G.,Russell, Linda J.,Stocker, Richard,Woolven, James M.
, p. 3037 - 3040 (2011)
Heteroalicyclic carboxamidines were synthesised and evaluated as inhibitors of nitric oxide synthases. (2R)-2-Pyrrolidinecarboxamidine, in particular, was shown to be a highly potent in vitro (IC50 = 0.12 μM) and selective iNOS inhibitor (>100-fold vs both eNOS and nNOS), with probable binding to the key anchoring glutamate residue and co-ordination to the haem iron.
