61495-03-2 Usage
Aromatic and heterocyclic
2-(1-Methyl-cyclohexyl)-1H-indole is a chemical compound known for its aromatic and heterocyclic properties.
Six-membered cyclohexyl ring
It consists of a six-membered cyclohexyl ring.
Methyl group attached
A methyl group is attached to one carbon atom of the cyclohexyl ring.
Indole ring system
The compound also contains an indole ring system.
Potential pharmacological effects
2-(1-Methyl-cyclohexyl)-1H-indole has been studied for its potential pharmacological effects in the field of medicinal chemistry.
Structure and reactivity
Its structure and reactivity make it an interesting molecule for drug development and research into the physiological effects of indole derivatives.
Building block in synthesis
Additionally, it is used as a building block in the synthesis of other organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 61495-03-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,4,9 and 5 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 61495-03:
(7*6)+(6*1)+(5*4)+(4*9)+(3*5)+(2*0)+(1*3)=122
122 % 10 = 2
So 61495-03-2 is a valid CAS Registry Number.
61495-03-2Relevant academic research and scientific papers
Lithiation of N-(2-Alkylphenyl)alkanamides and Related Compounds. A Modified Madelung Indole Synthesis
Houlihan, William J.,Parrino, Vincent A.,Uike, Yasuyuki
, p. 4511 - 4515 (2007/10/02)
A modified Madelung synthesis for the conversion of N-(alkylphenyl)alkanamides and related compounds to indoles, benzindoles, and azindoles has been developed.This procedure consists of treating the amide with 2 or 3 equiv of n-butyllithium or lithium diisopropylamide in tetrahydrofuran at temperatures from -20 to +25 deg C.Several examples where products other than indoles were formed from the starting amide are also reported.
2-Substituted indoles and process for their preparation
-
, (2008/06/13)
Highly branched α-substituted indoles, e.g., 2-(1-methylcyclohexyl)-indole, are prepared by treating N-(α-branched carbonyl) toluidines with alkyl lithium. The reaction sequence may be illustrated as SPC1
