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2-methyl-3-[(2-methyl-3H-indol-3-ylidene)methyl]-1H-indole is a complex organic compound with a molecular formula of C18H16N2. It is a derivative of indole, a heterocyclic aromatic organic compound that contains a benzene ring fused to a pyrrole ring. This specific compound features a methyl group at the 2nd position of the indole ring and a substituted indole group attached to the 3rd position through a methylene bridge. The substituted indole group itself has a methyl group at the 2nd position and a double bond between the 2nd and 3rd carbon atoms, forming a 3H-indol-3-ylidene structure. 2-methyl-3-[(2-methyl-3H-indol-3-ylidene)methyl]-1H-indole is of interest in the field of organic chemistry and may have potential applications in the synthesis of pharmaceuticals or other chemical products due to its unique structure and properties.

525-58-6

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525-58-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 525-58-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,2 and 5 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 525-58:
(5*5)+(4*2)+(3*5)+(2*5)+(1*8)=66
66 % 10 = 6
So 525-58-6 is a valid CAS Registry Number.

525-58-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Indole, 2-methyl-3-[(2-methyl-3H-indol-3-ylidene)methyl]-

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

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More Details:525-58-6 SDS

525-58-6Relevant academic research and scientific papers

A short, novel, and practical synthesis of 3-alkenylated indoles

Kargar, Mojgan,Hekmatshoar, Rahim,Mostashari, Abdol Jalil

, p. 1743 - 1749 (2013/05/21)

Direct metal-free alkenylation of 2-methylindole via acid-mediated Michael addition-elimination reaction with ethoxymethylenemalononitrile or ethyl ethoxymethylenecyanoacetate affords 3-indolyl-2-cyanoacrylonitrile and ethyl 3-indolyl-2-cyanoacrylate. Behavior of 1H-indole is predictably different. Copyright Taylor & Francis Group, LLC.

Synthesis of novel methylene bridge functionalized bis(indolyl)methanes thorough a double Michael addition

Kargar, Mojgan,Hekmatshoar, Rahim,Mostashari, Abdoljalil

experimental part, p. 2535 - 2546 (2012/01/13)

A simple synthesis of a series of novel diethyl bis(indol-3-yl)- methylmalonate is described. This involves domino Michael addition/elimination/ Michael addition of indoles to diethyl ethoxymethylenemalonate as double Michael acceptor.

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