81723-24-2 Usage
Chemical class
Tricarboxylate ester
Explanation
Derived from a carboxylic acid and contains three carboxylate functional groups.
Explanation
The molecule contains an azepine ring, which is a seven-membered nitrogen-containing ring.
Explanation
An ethyl group is attached to one of the nitrogen atoms in the azepine ring, and two methyl groups are attached to different carbon atoms in the ring.
Explanation
The molecule has three carboxylate functional groups, which are derived from the carboxylic acid.
Explanation
Tricarboxylate esters can exhibit a wide range of biological and chemical properties, making them potentially useful in these industries.
Explanation
Additional research and testing would be needed to validate and explore the specific uses and properties of 1-ethyl 2,5-dimethyl 1H-azepine-1,2,5-tricarboxylate.
Structure
Azepine ring
Substituents
Ethyl group and two methyl groups
Functional groups
Carboxylate groups
Potential applications
Pharmaceutical and chemical industries
Further research
Specific uses and properties
Check Digit Verification of cas no
The CAS Registry Mumber 81723-24-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,7,2 and 3 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 81723-24:
(7*8)+(6*1)+(5*7)+(4*2)+(3*3)+(2*2)+(1*4)=122
122 % 10 = 2
So 81723-24-2 is a valid CAS Registry Number.
81723-24-2Relevant academic research and scientific papers
Azides. Part IV. Thermolysis of ethyl azidoformate in dimethyl terephthalate; formation of a diazabicyclooctadiene heterocycle
Ayyangar, N. R.,Bambal, R. B.,Srinivasan, K. V.,Row, T. N. Guru,Puranik, V. G.,et al.
, p. 1969 - 1973 (2007/10/02)
Thermal decomposition of ethyl azidoformate in excess of dimethyl terephthalate (DMT) (1) in acetic anhydride as solvent results in the formation of N,N-dicarbethoxy-4,8-dicarbomethoxy-2,6-diazabicycloocta-3,7-diene (3) in addition to N-carbethoxy-2,5-dicarbomethoxy-1H-azepine (2) and ethyl-N-(2,5-dicarbomethoxyphenyl)carbamate (4).The structure of the diazabicyclooctadiene (3) was established on the basis of spectral, elemental, and X-ray crystallographic analyses.
FACILE SYNTHESIS OF N-SUBSTITUTED 1H-AZEPINE DERIVATIVES
Ayyangar, Nagaraj R.,Bambal, Ramesh B.,Lugade, Ananda G.
, p. 77 - 82 (2007/10/02)
The facile synthesis of N-sulphonyl and N-ethoxycarbonyl substituted 1H-azepines in high yields by the pressure-induced sulphonylnitrene insertion reaction or, in anhydrous solvents, the 1,3-dipolar azide addition reaction with aromatic substrates containing electron-withdrawing substituents (e.g. dimethyl terephthalate) are described.The probable sequences of reactions involved in the two cases have been indicated.
