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4H-Indol-4-one, 1,5,6,7-tetrahydro-2-methyl-3-phenyl- is a chemical compound belonging to the indole family, characterized by a unique structure and properties. 4H-Indol-4-one, 1,5,6,7-tetrahydro-2-methyl-3-phenyl- is a derivative of indole, with a 4H-oxindole core, which is a type of indole that contains a carbonyl group at the 4-position. The compound is further defined by its 1,5,6,7-tetrahydro structure, indicating that the molecule has four hydrogen atoms added across the 1,5,6, and 7 positions, leading to a reduction in the number of double bonds and an increase in the number of single bonds. Additionally, it features a methyl group at the 2-position and a phenyl group at the 3-position, which are substituents that significantly influence its chemical reactivity and physical properties. 4H-Indol-4-one, 1,5,6,7-tetrahydro-2-methyl-3-phenyl- is of interest in various fields, including pharmaceuticals and materials science, due to its potential applications in the development of new drugs and other chemical products.

6116-87-6

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6116-87-6 Usage

Molecular weight

213.27 g/mol
Used in organic synthesis and pharmaceutical research
Potential biological activities
Studied for potential use in treatment of diseases like cancer and neurodegenerative disorders
Possible applications in development of new drugs and therapeutic agents

Check Digit Verification of cas no

The CAS Registry Mumber 6116-87-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,1 and 6 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6116-87:
(6*6)+(5*1)+(4*1)+(3*6)+(2*8)+(1*7)=86
86 % 10 = 6
So 6116-87-6 is a valid CAS Registry Number.

6116-87-6Downstream Products

6116-87-6Relevant academic research and scientific papers

Catalyzed Reaction of Diazodiphenylethanone and Related Diazo Ketones with Enaminones as a Source of Pyrroles

Eberlin, Marcos N.,Kascheres, Concetta

, p. 2084 - 2086 (2007/10/02)

The reaction of copper(II)-stabilized keto carbenes (1, 7, 8), derived from diazo ketones, with enaminones leads to the formation of pyrroles.The cyclic enaminones 3 react with the keto carbenes on nitrogen to form products 5, 9, 11, and/or pyrroles 6, 10

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