93109-50-3 Usage
Heterocyclic compound
1H-Azepine-1,3-dicarboxylic acid is a derivative of azepine, which is an organic compound containing a ring of carbon and nitrogen atoms.
Amino group
The presence of an amino group (-NH2) contributes to the compound's potential biological and pharmaceutical applications.
Cyano group
The cyano group (-CN) is a nitrogen-carbon triple bond that may contribute to the compound's chemical reactivity and potential applications.
Phenyl ring
The phenyl ring (a six-carbon ring with delocalized electrons) is a common structural feature in many biologically active compounds and may contribute to the compound's pharmacological properties.
Ethyl and methyl ester groups
The addition of an ethyl (-CH2-CH3) and a methyl ester (-COOCH3) group enhances the compound's solubility and stability, making it more suitable for use in drug development.
Potential pharmacological properties
The structural features of 1H-Azepine-1,3-dicarboxylic acid, 2-amino-5-cyano-6,7-dihydro-6-phenyl-, 1-ethyl 3-methyl ester suggest that it may have potential pharmacological properties, but further research and testing are needed to confirm this.
Synthesis of new pharmaceutical agents
The compound could be useful in the synthesis of new pharmaceutical agents with diverse biological activities, but more research is needed to fully understand its potential applications.
Check Digit Verification of cas no
The CAS Registry Mumber 93109-50-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,1,0 and 9 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 93109-50:
(7*9)+(6*3)+(5*1)+(4*0)+(3*9)+(2*5)+(1*0)=123
123 % 10 = 3
So 93109-50-3 is a valid CAS Registry Number.
93109-50-3Relevant academic research and scientific papers
Studies on Heterocyclic Enaminonitriles. V. Reactions of 2-Amino-3-cyano-1-ethoxycarbonyl-4,5-dihydropyrroles with Acetylenic Esters
Matsunaga, Hisashi,Sonoda, Miki,Tomioka, Yukihiko,Yamazaki, Motoyoshi
, p. 2596 - 2601 (2007/10/02)
The reactions of 2-amino-3-cyano-1-ethoxycarbonyl-4,5-dihydropyrrole (Ia) and 2-amino-3-cyano-1-ethoxycarbonyl-5-methyl(or 4-phenyl)-4,5-dihydropyrrole (Ib or Ic) with dimethyl acetylenedicarboxylate and methyl propiolate gave the corresponding 7-amino-4-
