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1,4-Cyclohexadiene-1-carboxylic acid, 2-(1H-indol-3-yl)-3,6-dioxo-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

63579-42-0

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63579-42-0 Usage

Chemical structure

A complex structure containing a cyclohexadiene carboxylic acid moiety and an indole group.

Functional groups

Carboxylic acid, ester, cyclohexadiene, and indole.

Type of ester

Methyl ester, derived from the reaction of the compound's carboxylic acid group with methanol.

Molecular weight

Approximately 269.27 g/mol (calculated from the molecular formula).

Appearance

Likely a solid or viscous liquid, depending on the conditions (not specified in the material).

Solubility

Soluble in organic solvents like methanol, ethanol, and acetone (not specified in the material, but typical for similar structures).

Stability

May be sensitive to heat, light, and moisture (not specified in the material, but a general consideration for compounds with ester and indole groups).

Applications

Potential uses in pharmaceuticals, agrochemicals, and materials sciences.

Check Digit Verification of cas no

The CAS Registry Mumber 63579-42-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,5,7 and 9 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 63579-42:
(7*6)+(6*3)+(5*5)+(4*7)+(3*9)+(2*4)+(1*2)=150
150 % 10 = 0
So 63579-42-0 is a valid CAS Registry Number.

63579-42-0Downstream Products

63579-42-0Relevant academic research and scientific papers

Bimetallic copper/cobalt-cocatalyzed double aerobic phenol oxidation/cyclization toward π-extended benzofuro[2,3-b]indoles as electron donors for electroluminescence

Bashir, Muhammad Adnan,Zhang, Yulong,Yu, Huaibin,Wang, Bofei,Zhao, Weining,Zhong, Fangrui

, p. 5031 - 5036 (2021)

Benzofuro[2,3-b]indoles, apart from their attractive biological features, constitute a novel family of electron donors for electroluminescent materials. Reported herein is the establishment of a strategy involving bimetallic catalysis to form such π-conju

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