94940-87-1 Usage
Molecular structure
1H-Indeno[1,2-b]pyridine-3-carboxylic acid, 4,4a,5,9b-tetrahydro-2,4a-dimethyl-5-oxo-4-phenyl-, ethyl ester is a complex organic compound with a specific molecular structure that includes a combination of various functional groups.
Ethyl ester derivative
The compound is an ethyl ester derivative of 1H-Indeno[1,2-b]pyridine-3-carboxylic acid, which means it has an ester functional group formed by the reaction of the carboxylic acid with ethanol.
Carbonyl and phenyl groups
The presence of a carbonyl group (C=O) and a phenyl group (C6H5) in the compound suggests its potential role as a pharmaceutical or organic intermediate due to the reactivity and versatility of these functional groups.
Pharmaceutical and chemical applications
Given its complex structure and potential functional groups, the compound is likely to have specific applications in the pharmaceutical or chemical industry. Further studies and analyses would be required to determine its specific uses and properties.
Require further research
The compound's long chemical name and complex structure indicate that it may have unique properties and potential applications. However, more research and analysis are needed to fully understand its behavior and potential uses.
Check Digit Verification of cas no
The CAS Registry Mumber 94940-87-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,9,4 and 0 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 94940-87:
(7*9)+(6*4)+(5*9)+(4*4)+(3*0)+(2*8)+(1*7)=171
171 % 10 = 1
So 94940-87-1 is a valid CAS Registry Number.
94940-87-1Relevant academic research and scientific papers
Synthesis and isomerization of 1H-4,4a,5,9b-tetrahydroindeno-[1,2-b]pyridines
Lusis,Muceniece,Stonkuss,Duburs
, p. 7429 - 7436 (2007/10/02)
Synthesis of 1H-4,4a,5,9b-tetrahydroindeno[1,2-b]pyridines has been accomplished by catalytic hydrogenation of 4H-4a,5-dihydroindenopyridines. The isomerization of 1H-4,4a,5,9b-tetrahydroindenopyridines containing an acyl function at C-3 leads to 3H-4,4a,
STRUCTURE AND PROPERTIES OF 2,4a-DIMETHYL-4-PHENYL-3-ETHOXYCARBONYL-5-OXO-4a,5-DIHYDRO-4H-INDENOPYRIDINE
Bundule, M. F.,Mishnev, A. F.,Bleidelis, Ya. Ya.,Lusis, V. K.,Mutsenietse, D. Kh.,Dubur, G. Ya.
, p. 1145 - 1149 (2007/10/02)
The molecular and crystal structure of 2,3a-dimethyl-4-phenyl-3-ethoxycarbonyl-5-oxo-4a,5-dihydro-4H-indenopyridine has been determined, and its reduction and alkaline and acid hydrolysis reactions have been studied.
