959395-07-4 Usage
Description
(?)?2?(((S)?2?((S)?1?(pyridin?2?ylmethyl)pyrrolidin?2?yl)pyrrolidin?1?yl)methyl)pyridine is a complex chiral molecule composed of multiple pyrrolidine and pyridine rings interconnected through carbon chains. The presence of "S" and "(?)" symbols indicates multiple stereocenters, which are essential for its three-dimensional structure. The pyridine and pyrrolidine moieties within this compound are commonly found in pharmaceuticals and biologically active molecules, suggesting potential applications in the medical and chemical fields. Further chemical and biological studies are required to determine the specific properties and activities of this compound.
Uses
Used in Pharmaceutical Development:
(?)?2?(((S)?2?((S)?1?(pyridin?2?ylmethyl)pyrrolidin?2?yl)pyrrolidin?1?yl)methyl)pyridine is used as a potential candidate in pharmaceutical development due to its complex structure and the presence of biologically active functional groups. The chiral nature of the compound may offer selectivity in drug-target interactions, which is crucial for the development of effective medications with fewer side effects.
Used in Chemical Research:
In the field of chemical research, (?)?2?(((S)?2?((S)?1?(pyridin?2?ylmethyl)pyrrolidin?2?yl)pyrrolidin?1?yl)methyl)pyridine can be utilized for studying the synthesis and properties of complex organic molecules. Its unique structure may provide insights into new reaction pathways and mechanisms, contributing to the advancement of organic chemistry.
Used in Biological Studies:
(?)?2?(((S)?2?((S)?1?(pyridin?2?ylmethyl)pyrrolidin?2?yl)pyrrolidin?1?yl)methyl)pyridine may also be employed in biological studies to explore its interactions with various biological targets. The presence of pyridine and pyrrolidine rings could potentially allow the compound to bind to specific receptors or enzymes, making it a candidate for investigating its effects on biological processes.
Used in Material Science:
(?)?2?(((S)?2?((S)?1?(pyridin?2?ylmethyl)pyrrolidin?2?yl)pyrrolidin?1?yl)methyl)pyridine's unique structure and chiral properties may also find applications in material science. It could be used to develop new materials with specific properties, such as chiral catalysts, sensors, or other functional materials that exploit the compound's structural features for technological applications.
Check Digit Verification of cas no
The CAS Registry Mumber 959395-07-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,9,3,9 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 959395-07:
(8*9)+(7*5)+(6*9)+(5*3)+(4*9)+(3*5)+(2*0)+(1*7)=234
234 % 10 = 4
So 959395-07-4 is a valid CAS Registry Number.
959395-07-4Relevant articles and documents
H2O2 activation with biomimetic non-haem iron complexes and AcOH: Connecting the g = 2.7 EPR signal with a visible chromophore
Makhlynets, Olga V.,Oloo, Williamson N.,Moroz, Yurii S.,Belaya, Irina G.,Palluccio, Taryn D.,Filatov, Alexander S,Mueller, Peter,Cranswick, Matthew A.,Que, Lawrence,Rybak-Akimova, Elena V.
, p. 645 - 648 (2014)
Mechanistic studies of H2O2 activation by complexes related to [(BPMEN)FeII(CH3CN)2]2+ with electron-rich pyridines revealed that a new intermediate formed in the presence of acetic acid with a 465 nm visible band can be associated with an unusual g = 2.7 EPR signal. We postulate that this chromophore is an acylperoxoiron(iii) intermediate.
Effects of denticity and ligand rigidity on reactivity of copper complexes with cumyl hydroperoxide
Pella, Bruce J.,Niklas, Jens,Poluektov, Oleg G.,Mukherjee, Anusree
, p. 71 - 78 (2018/08/21)
Cu(II) complexes bearing N2/Py2 tetradentate ligands consisting of two pyridyl arms and a flexible ethyldiamine backbone, [(BPMEN)Cu(ClO4)2] (1), with rigid cyclohexyl backbone [(BPMCN)Cu(ClO4)2] (2), and substituted with bispyrrolidyl [(PDP)Cu(ClO4)2] (3), and Cu(II) complex bearing N2/Py3 pentadentate ligand, [(TPMEN)Cu(ClO4)2] (4), were synthesized and structurally characterized. Reactivity of 1–4 with cumyl hydroperoxide was investigated to study the effects of ligand rigidity and denticity on the mechanism of O–O bond cleavage. Results presented herein illustrate that 1–3 favors homolysis, however 4 showed little to almost no impact on O–O bond cleavage.
Asymmetric epoxidation with H2O2 by manipulating the electronic properties of non-heme iron catalysts
Cusso, Olaf,Garcia-Bosch, Isaac,Ribas, Xavi,Lloret-Fillol, Julio,Costas, Miquel
supporting information, p. 14871 - 14878 (2013/10/22)
A non-heme iron complex that catalyzes highly enantioselective epoxidation of olefins with H2O2 is described. Improvement of enantiomeric excesses is attained by the use of catalytic amounts of carboxylic acid additives. Electronic effects imposed by the ligand on the iron center are shown to synergistically cooperate with catalytic amounts of carboxylic acids in promoting efficient O-O cleavage and creating highly chemo-and enantioselective epoxidizing species which provide a broad range of epoxides in synthetically valuable yields and short reaction times.
