389092-25-5 Usage
Uses
Used in Pharmaceutical Industry:
1(2H)-Pyridinecarboxylic acid, 3,4-dihydro-4-oxo-2-[(phenylmethoxy)methyl]-, phenylmethyl ester, (2S)is used as a pharmaceutical intermediate for the synthesis of various drugs. Its unique structural features, including the pyridine ring, carboxylic acid group, and phenylmethyl ester group, make it a promising candidate for the development of new medications.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 1(2H)-Pyridinecarboxylic acid, 3,4-dihydro-4-oxo-2-[(phenylmethoxy)methyl]-, phenylmethyl ester, (2S)is utilized for studying the structure-activity relationships of biologically active compounds. The presence of common pharmacophore elements, such as the phenyl group and ester moiety, allows researchers to explore its potential in designing new drugs with improved efficacy and selectivity.
Used in Drug Design and Optimization:
1(2H)-Pyridinecarboxylic acid,
3,4-dihydro-4-oxo-2-[(phenylmethoxy)methyl]-, phenylmethyl ester, (2S)-'s structural characteristics make it a valuable tool in drug design and optimization processes. By incorporating elements from 1(2H)-Pyridinecarboxylic acid, 3,4-dihydro-4-oxo-2-[(phenylmethoxy)methyl]-, phenylmethyl ester, (2S)into new drug candidates, chemists can potentially enhance the pharmacological properties of these molecules, leading to more effective treatments for various diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 389092-25-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,9,0,9 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 389092-25:
(8*3)+(7*8)+(6*9)+(5*0)+(4*9)+(3*2)+(2*2)+(1*5)=185
185 % 10 = 5
So 389092-25-5 is a valid CAS Registry Number.
389092-25-5Relevant academic research and scientific papers
Enantiopure 2,3-dihydro-4-pyridones as synthetic intermediates: Asymmetric synthesis of 1-deoxynojirimycin
Comins, Daniel L,Fulp, Alan B
, p. 6839 - 6841 (2007/10/03)
An asymmetric synthesis of 1-deoxynojirimycin (2) mediated by a chiral auxiliary is reported. The dihydropyridone 4 was converted to diol 11 in three steps by acetoxylation, hydrolysis, and stereoselective reduction. Dihydroxylation of 11 followed by catalytic reduction afforded 2.
