7063-73-2 Usage
Molecular structure
A complex chemical compound with a long molecular structure.
1,3-thiazolidin-3-yl ring
A heterocyclic ring system containing sulfur and nitrogen atoms.
1,6-dihydropyridin-3-yl group
A six-membered nitrogen-containing ring with one double bond.
3,5-dimethylpiperidin-1-yl substituent
A piperidine ring with two methyl groups at positions 3 and 5.
2-thioxo-1-thiazolidin-3-yl moiety
A five-membered ring containing sulfur and nitrogen atoms.
Cyano group
A carbon-nitrogen triple bond (C≡N) functional group.
Ethyl group
A two-carbon alkyl group (-CH2CH3).
Piperidin-1-yl group
A six-membered nitrogen-containing ring with a single bond to the rest of the molecule.
Potential applications
Pharmaceutical or biological applications, possibly as a drug or a molecular probe in biological research.
Further study needed
Characterization of properties and potential uses to understand capabilities and limitations.
11-(5-{[5-cyano-2-(3,5-dimethylpiperidin-1-yl)-1-ethyl-4-methyl-6-oxo-1,6-dihydropyridin-3-yl]methylidene}-4-oxo-2-thioxo-1,3-thiazolidin-3-yl)undecanoic acid's complex structure and the presence of multiple functional groups suggest that it may have unique properties and potential applications in various fields. Further research and characterization are necessary to fully explore its potential.
Check Digit Verification of cas no
The CAS Registry Mumber 7063-73-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,6 and 3 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7063-73:
(6*7)+(5*0)+(4*6)+(3*3)+(2*7)+(1*3)=92
92 % 10 = 2
So 7063-73-2 is a valid CAS Registry Number.
7063-73-2Relevant academic research and scientific papers
One-pot preparation of arylethynyl sulfides and bis(arylethynyl) sulfides
Su, Qiong,Zhao, Zi-Jian,Xu, Feng,Lou, Peng-Cai,Zhang, Kai,Xie, De-Xun,Shi, Lei,Cai, Qing-Yun,Peng, Zhi-Hong,An, De-Lie
, p. 1551 - 1557 (2013/04/23)
An efficient preparation for arylethynyl sulfides 1 and bis(arylethynyl) sulfides 2 has been accomplished through a one-pot, three-step strategy that starts from arylethanonyl sulfides and bis(arylethanonyl) sulfides, respectively, without the use of various terminal arylacetylenes as substrates. When lithium hexamethyldisilazane (LHMDS), ClP(O)(OEt)2, and LHMDS were sequentially added to a tetrahydrofuran solution of different substrates [arylethanonyl sulfides or bis(arylethanonyl) sulfides], 1 or 2 were obtained in moderate to good yields. The reaction procedure involves the formation of an enol phosphate and a subsequent base-induced elimination. An efficient preparation of arylethynyl sulfides 1 and bis(arylethynyl) sulfides 2 has been accomplished by a one-pot, three-step strategy that starts from arylethanonyl sulfides and bis(arylethanonyl) sulfides, respectively, to give 1 and 2 in moderate to good yields. The reaction mechanism involves the formation of an enol phosphate that undergoes a subsequent base-induced elimination. Copyright
