230309-12-3 Usage
Chemical structure
The compound has a complex structure that includes a pyridine ring, a phenylmethyl group, and a thiazolidinylcarbonyl group.
Functional groups
It contains a methyl ester functional group.
Configuration
The compound is in the (4R)configuration.
Potential applications
It may have potential pharmaceutical or biological applications due to the presence of the thiazolidinylcarbonyl group, which is known for its diverse biological activities.
Interactions with biological systems
The presence of the phenylmethyl group suggests potential interactions with biological systems.
Further research
Further research is needed to fully understand the properties and potential uses of 1(4H)-Pyridinecarboxylic acid,
4-(phenylmethyl)-3-[[(4S)-4-phenyl-2-thioxo-3-thiazolidinyl]carbonyl]-,
methyl ester, (4R)-.
Check Digit Verification of cas no
The CAS Registry Mumber 230309-12-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,0,3,0 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 230309-12:
(8*2)+(7*3)+(6*0)+(5*3)+(4*0)+(3*9)+(2*1)+(1*2)=83
83 % 10 = 3
So 230309-12-3 is a valid CAS Registry Number.
230309-12-3Relevant academic research and scientific papers
Regio- and stereoselective synthesis of 1,4-dihydropyridines by way of an intramolecular interaction of a thiocarbonyl or carbonyl with a pyridinium nucleus
Yamada, Shinji,Misono, Tomoko,Ichikawa, Mayumi,Morita, Chisako
, p. 8939 - 8949 (2007/10/03)
Chiral 1,4-dihydropyridines were prepared by the regio- and stereoselective addition of ketene silyl acetals and organometallic reagents to pyridinium salts. In the addition reaction, an intramolecular interaction between the thiocarbonyl or carbonyl with
Synthesis of chiral 1,4-dihydropyridines by diastereoface-selective asymmetric addition to nicotinic amides
Yamada, Shinji,Ichikawa, Mayumi
, p. 4231 - 4234 (2007/10/03)
Diastereoface-selective asymmetric addition of organometallic reagents to pyridinium salts of 1 and 2 was performed to give chiral 1,4-dihydropyridines in good regio- and stereoselectivities. The absolute configuration of the newly-produced chiral center
