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4H-Indol-4-one, 1,5,6,7-tetrahydro-3-methyl-2-phenyl- is a complex organic compound belonging to the indole family. It is characterized by a unique molecular structure, with a 4H-indol-4-one core, which features a 1,5,6,7-tetrahydro ring system, a 3-methyl group, and a 2-phenyl substituent. 4H-Indol-4-one, 1,5,6,7-tetrahydro-3-methyl-2-phenyl- is primarily used in the synthesis of various pharmaceuticals and agrochemicals due to its versatile chemical properties and potential biological activities. Its chemical formula is C14H15NO, and it has a molecular weight of 211.27 g/mol. The compound's structure and properties make it an interesting target for researchers in the fields of medicinal chemistry and drug discovery.

6116-85-4

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6116-85-4 Usage

Main properties

1. Chemical compound
2. Belongs to the class of indolones
3. Derivative of 4H-indol-4-one
4. Tetrahydro structure
5. Methyl group at position 3
6. Phenyl group at position 2
7. Potential pharmacological activities
8. Anti-inflammatory properties
9. Analgesic properties
10. Potential applications in drug development
11. Importance in medicinal chemistry
12. Research interest in chemical and biological properties

Specific content

Presence of tetrahydro structure
Methyl group at position 3
Phenyl group at position 2
Potential pharmacological activities
Anti-inflammatory and analgesic properties
Applications in drug development
Importance in medicinal chemistry
Need for further research in chemical and biological properties.

Check Digit Verification of cas no

The CAS Registry Mumber 6116-85-4 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 5 respectively.
Calculate Digit Verification of CAS Registry Number 6116-85:
(6*6)+(5*1)+(4*1)+(3*6)+(2*8)+(1*5)=84
84 % 10 = 4
So 6116-85-4 is a valid CAS Registry Number.

6116-85-4Downstream Products

6116-85-4Relevant 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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