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1-(5-Hydroxy-2-methyl-1-phenyl-1H-indol-3-yl)-ethanone is a complex organic compound with the molecular formula C17H15NO2. It is a derivative of indole, a heterocyclic aromatic organic compound, and features a hydroxyl group (-OH) at the 5-position, a methyl group (-CH3) at the 2-position, and a phenyl group (C6H5) at the 1-position. The compound also has a ketone functional group (C=O) attached to the ethanone (CH3CO) moiety. This molecule is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its role as an intermediate in the production of certain dyes and pigments. Its chemical structure and properties make it a versatile building block in organic synthesis, with potential applications in the development of new drugs and other chemical products.

5102-18-1

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5102-18-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5102-18-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,0 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5102-18:
(6*5)+(5*1)+(4*0)+(3*2)+(2*1)+(1*8)=51
51 % 10 = 1
So 5102-18-1 is a valid CAS Registry Number.
InChI:InChI=1/C17H15NO2/c1-11-17(12(2)19)15-10-14(20)8-9-16(15)18(11)13-6-4-3-5-7-13/h3-10,20H,1-2H3

5102-18-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(5-HYDROXY-2-METHYL-1-PHENYL-1H-INDOL-3-YL)-ETHANONE

1.2 Other means of identification

Product number -
Other names 3-acetyl-5-hydroxy-2-methyl-1-phenylindole

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

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5102-18-1 SDS

5102-18-1Relevant academic research and scientific papers

Montmorillonite clay catalyzed three component, one-pot synthesis of 5-Hydroxyindole derivatives

Reddy, B.V.Subba,Reddy, P. Sivaramakrishna,Reddy, Y. Jayasudhan,Bhaskar,Reddy, B. Chandra Obula

, p. 2968 - 2972 (2014/01/06)

A highly efficient and environmentally benign protocol has been developed for the first time to produce a wide range of biologically active 5-hydroxyindole derivatives using montmorillonite KSF clay as a reusable solid acid catalyst. The use of recyclable clay makes this procedure quite simple, more convenient and cost-effective.

Lewis acid catalyzed Nenitzescu indole synthesis

Velezheva, Valeriya S.,Kornienko, Albert G.,Topilin, Sergey V.,Turashev, Ascar D.,Peregudov, Alexander S.,Brennan, Patrick J.

, p. 873 - 879 (2007/10/03)

A novel method for Lewis acid catalyzed Nenitzescu indole syntheses of 5-hydroxyindoles bearing different substituents in positions 1 (Alk, Bn, Ar), 2 (Me, Et, Ph), and 3 (COOEt, COMe, CONHPh) as well as tricyclic derivatives are reported. The method is simple, rapid, efficient, and allows preparation of hydroxyindoles from 1,4-benzoquinone and enamines in good to excellent yields with the use of low-polar solvents in the presence of weak Lewis acids catalysts. The formation of 5-hydroxyindoles under such mild conditions is explained in terms of a non-redox mechanism.

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