138135-48-5 Usage
Description
Ethyl 4-(3-Aminophenyl)-5-(Methoxycarbonyl)-2,6-dimethyl-1,4-dihydropyridine-3-carboxylate is a complex chemical compound belonging to the dihydropyridine class. It features a unique molecular structure with ethyl, amino, methoxycarbonyl, and dimethyl functional groups, which may contribute to its potential biological activity and therapeutic applications. Ethyl 4-(3-AMinophenyl)-5-(Methoxycarbonyl)-2,6-diMethyl-1,4-dihydropyridine-3-carboxylate is of interest in the pharmaceutical and agrochemical industries due to its possible uses in drug development and other applications.
Uses
Used in Pharmaceutical Industry:
Ethyl 4-(3-Aminophenyl)-5-(Methoxycarbonyl)-2,6-dimethyl-1,4-dihydropyridine-3-carboxylate is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure and functional groups make it a valuable component in the development of new drugs with potential therapeutic benefits.
Used in Agrochemical Industry:
In the agrochemical sector, Ethyl 4-(3-Aminophenyl)-5-(Methoxycarbonyl)-2,6-dimethyl-1,4-dihydropyridine-3-carboxylate is utilized as a precursor in the production of agrochemicals. Its properties may contribute to the creation of effective pesticides, herbicides, or other agricultural chemicals that can enhance crop protection and yield.
Used in Drug Development Research:
Ethyl 4-(3-AMinophenyl)-5-(Methoxycarbonyl)-2,6-diMethyl-1,4-dihydropyridine-3-carboxylate is also used as a research target in drug development. Its complex structure and potential biological activity make it a promising candidate for the discovery of new therapeutic agents, particularly in the areas of cardiovascular, neurological, or other medical fields where dihydropyridine-based drugs have shown efficacy.
Used in Chemical Synthesis:
Ethyl 4-(3-Aminophenyl)-5-(Methoxycarbonyl)-2,6-dimethyl-1,4-dihydropyridine-3-carboxylate serves as a versatile building block in chemical synthesis. Its functional groups can be modified or used as starting points for the creation of a wide range of chemical products, including specialty chemicals, materials, or other complex organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 138135-48-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,1,3 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 138135-48:
(8*1)+(7*3)+(6*8)+(5*1)+(4*3)+(3*5)+(2*4)+(1*8)=125
125 % 10 = 5
So 138135-48-5 is a valid CAS Registry Number.
138135-48-5Relevant articles and documents
Dihydropyridine neuropeptide Y Y1 receptor antagonists
Poindexter, Graham S.,Bruce, Marc A.,LeBoulluec, Karen L.,Monkovic, Ivo,Martin, Scott W.,Parker, Eric M.,Iben, Larry G.,McGovern, Rachel T.,Ortiz, Astrid A.,Stanley, Jennifer A.,Mattson, Gail K.,Kozlowski, Michael,Arcuri, Meredith,Antal-Zimanyi, Ildiko
, p. 379 - 382 (2007/10/03)
Dihydropyridine 5a was found to be an inhibitor of neuropeptide Y1 binding in a high throughput 125I-PYY screening assay. Structure-activity studies around certain portions of the dihydropyridine chemotype identified BMS-193885 (6e)
DIHYDROPYRIDINE NPY ANTAGONISTS: PIPERIDINE DERIVATIVES
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, (2008/06/13)
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Process for preparation of enantiomerically pure polysubstituted 1,4-dihydropyridines
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, (2008/06/13)
A process for the optical resolution of racemic 1,4-dihydropyridines, containing isothioureido groups. Salification of racemic isothioureas with optically active acids produces diasteroisomeric mixtures of isothiouronium salts, that, using conventional techniques, are separated in the individual components to give optically pure isothioureides of 1,4-dihydropyridines and salts thereof with conventional acids. Said optically pure 1,4-dihydropyridines can then be subjected to desulphuration and to different transformations to give to other enantiomerically pure and therapeutically useful 1,4-dihydropyridines.
