77871-94-4 Usage
Functional groups
The compound contains a ketone group (1-butanone) which is a carbonyl group (C=O) bonded to two alkyl or aryl groups, and a fluorophenyl group which is a phenyl ring with one or more fluorine atoms attached.
Heterocyclic ring system
The compound features a complex heterocyclic ring system with an imidazo and pyrido group, which are both nitrogen-containing heterocyclic rings. The imidazo ring is a five-membered ring with two nitrogen atoms, while the pyrido ring is a six-membered ring with one nitrogen atom.
Tetrahydro prefix
The "tetrahydro" prefix indicates that the compound has four hydrogen atoms added to the core structure of the heterocyclic ring system, which suggests a partially saturated and more stable structure.
Complexity
The compound's name and structure are highly specific and complex, indicating that it may have specialized properties and functions that are not found in simpler compounds.
Further research needed
Due to the compound's complexity and unique structure, additional research and analysis are necessary to fully understand its properties, applications, and potential uses in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 77871-94-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,8,7 and 1 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 77871-94:
(7*7)+(6*7)+(5*8)+(4*7)+(3*1)+(2*9)+(1*4)=184
184 % 10 = 4
So 77871-94-4 is a valid CAS Registry Number.
77871-94-4Relevant academic research and scientific papers
Agents Acting on CNS: Part XXXI - Synthesis of 2-Substituted 1,2,3,5,11,11a-Hexahydro-6H-imidazopyridoindoles
Kumar, Naresh,Dhaon, Madhup K.,Agrawal, Shiv K.,Saxena, Anil K.,Jain, Padam C.,Anand, Nitya
, p. 1087 - 1088 (2007/10/02)
The title compounds have been prepared starting from methyl 1,2,3,4-tetrahydropyridoindole-3-carboxylate (1).Treatment of 1 with methanolic solution of ammonia and methylamine affords the amides 5 and 6 respectively which furnish the corresponding amines 9 and 10 by LiAlH4 reduction. 5 and 6 on treatment with HCHO gives 2-substituted oxoimidazopyridoindoles (7,8) while 9 and 10 give imidazopyridoindoles (11,12).Treatment of 9, 10 with carbon disulphide gives the 3-thio derivates (13,14). 9 on condensation with γ-chloro-p-fluorobutyrophenone furnishes 15, which on ring closure with HCHO affords 2-γ-(p-fluorobenzoyl)propyl-1,2,3,5,11,11a-hexahydroimidazopyridoindole (16).None of these compounds exhibits any noteworthy biological activity.
