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Trimethyl 1H-Indole-4,6,7-tricarboxylate is a complex organic compound with the molecular formula C14H13NO6. It is characterized by a tricyclic structure, with an indole ring system at its core, and three carboxyl groups (-COOH) attached to the 4, 6, and 7 positions. The molecule also features three methyl groups (-CH3) attached to the nitrogen atom of the indole ring. Trimethyl 1H-Indole-4,6,7-tricarboxylate is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as in the development of new materials. Its unique structure and properties make it a subject of interest in organic chemistry and related fields.

86012-84-2

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86012-84-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86012-84-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,0,1 and 2 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 86012-84:
(7*8)+(6*6)+(5*0)+(4*1)+(3*2)+(2*8)+(1*4)=122
122 % 10 = 2
So 86012-84-2 is a valid CAS Registry Number.

86012-84-2Downstream Products

86012-84-2Relevant articles and documents

Diels-Alder Reactions of Vinyl Derivatives of Five-Membered Monoheterocyclic Compounds

Noland, Wayland E.,Lee, Chang Kiu,Bae, Sun Kun,Chung, Bong Yul,Hahn, Chi Sun,Kim, Keun Jae

, p. 2488 - 2491 (2007/10/02)

Vinylpyrroles having electron-withdrawing substituents react with dienophiles to give ? adducts while the furan and thiophene analogues do not.The difference in reactivity among the monoheterocycles can be explained in terms of the greater electron-releasing ability of the nitrogen atom in the pyrrole.The s-cis conformation of the (1H-pyrrol-2-yl)maleate derivatives appears to be an important factor in their undergoing the cycloaddition reaction.

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