230309-18-9 Usage
Uses
Used in Pharmaceutical Research:
3-Piperidinecarboxylic acid, 4-phenyl-, methyl ester, (3R,4R)is used as a research compound for exploring its potential biological activities and pharmacological properties. The stereochemistry at the 3R and 4R positions plays a crucial role in determining its specific biological and pharmacological effects, making it a valuable tool in drug discovery and development.
Used in Organic Chemistry:
In the field of organic chemistry, 3-Piperidinecarboxylic acid, 4-phenyl-, methyl ester, (3R,4R)serves as a versatile building block or intermediate for the synthesis of various complex organic molecules. Its unique structure and functional groups enable it to be used in the preparation of a wide range of chemical compounds, including pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Medicinal Chemistry:
3-Piperidinecarboxylic acid, 4-phenyl-, methyl ester, (3R,4R)is employed as a key component in the design and synthesis of novel therapeutic agents. Its unique structural features and stereochemistry make it a promising candidate for the development of new drugs with improved efficacy, selectivity, and safety profiles. Researchers can leverage its properties to create innovative pharmaceuticals targeting various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 230309-18-9 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 8 respectively.
Calculate Digit Verification of CAS Registry Number 230309-18:
(8*2)+(7*3)+(6*0)+(5*3)+(4*0)+(3*9)+(2*1)+(1*8)=89
89 % 10 = 9
So 230309-18-9 is a valid CAS Registry Number.
230309-18-9Relevant 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
