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Tris-(N-methylindol-3-yl)methane, also known as 1,3,5-trimethyl-2,4,6-tris(1H-indol-3-yl)benzene, is a trivalent organic compound with the molecular formula C27H22N3. It is a derivative of methane, where three N-methylindole groups are attached to the carbon atoms at positions 1, 3, and 5. tris-(N-methylindol-3-yl)methane is characterized by its unique structure, featuring a central benzene ring with three methylindole moieties attached to it. It is known for its potential applications in various fields, including materials science and pharmaceuticals, due to its interesting electronic and optical properties. The compound is also of interest in the study of supramolecular chemistry, as it can form complexes with other molecules through non-covalent interactions.

27065-95-8

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27065-95-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27065-95-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,0,6 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 27065-95:
(7*2)+(6*7)+(5*0)+(4*6)+(3*5)+(2*9)+(1*5)=118
118 % 10 = 8
So 27065-95-8 is a valid CAS Registry Number.

27065-95-8Downstream Products

27065-95-8Relevant academic research and scientific papers

NH4Cl-promoted synthesis of symmetrical and unsymmetrical triindolylmethanes under solvent-free conditions

Naskar, Subhendu,Hazra, Abhijit,Priyankar Paira,Sahu, Rishnendu B.,Banerjee, Sukdeb,Mondal, Nirup B.

experimental part, p. 568 - 571 (2009/09/25)

The synthesis of various triindolylmethanes from indole-3-carboxaldehyde, using indole derivatives as reactants and NH4Cl as catalyst under solvent-free conditions, is described. This methodology provides access to both symmetrical and unsymmetrical triindolylmethanes in excellent yields. With N-methylindole particularly, indole-3-carboxaldehyde appears to act as a formyl donor, leading to the exclusive formation of a symmetrically trisubstituted product. The novelty of the methodology lies in its operational simplicity, environment friendly reaction conditions, and inexpensive and easy availability of the catalyst. A plausible mechanism of formation of the products is suggested.

Novel clay-mediated, tandem addition-elimination-(Michael) addition reactions of indoles with 3-formylindole: An eco-friendly route to symmetrical and unsymmetrical triindolylmethanes

Chakrabarty, Manas,Sarkar, Sandipan

, p. 1351 - 1353 (2007/10/03)

Dry reaction of 3-formylindole (1) with indole (2a) on Montmorillonite K10 clay at room temperature furnished within minutes tris(indol-3-yl)methane (3a) in high yield. The reaction of 1 with other mono- and dialkylindoles (2b-c, skatole, 8a-c) under simi

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