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1-Propanone, 3-(4-methoxyphenyl)-3-(1-methyl-1H-indol-3-yl)-1-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

5883-78-3

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5883-78-3 Usage

Ketone derivative

The compound is a modified version of a ketone, which is a class of organic compounds characterized by the presence of a carbonyl group (C=O) bonded to two carbon-containing groups.

Propanone group

The compound is composed of a propanone group, which is a three-carbon chain with a carbonyl group at one end.

Additional phenyl group

The compound has a phenyl group (a six-carbon ring with delocalized electrons) attached to the propanone group, which can influence its chemical and physical properties.

Methyl group

The compound has a methyl group (a carbon atom bonded to three hydrogen atoms) attached to the compound's structure, which can affect its reactivity and solubility.

Methoxyphenyl group

The compound has a methoxyphenyl group (a phenyl ring with an attached methoxy group) attached to its structure, which can influence its chemical and biological properties.

Indolyl group

The compound has an indolyl group (a bicyclic structure with a nitrogen atom in the ring) attached to its structure, which can indicate its potential involvement in biological and pharmaceutical applications.

Diverse chemical and biological activities

The compound's complex structure suggests that it may have a range of chemical and biological activities, making it potentially useful in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 5883-78-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,8 and 3 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5883-78:
(6*5)+(5*8)+(4*8)+(3*3)+(2*7)+(1*8)=133
133 % 10 = 3
So 5883-78-3 is a valid CAS Registry Number.

5883-78-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-methoxyphenyl)-3-(1-methylindol-3-yl)-1-phenylpropan-1-one

1.2 Other means of identification

Product number -
Other names 1-Propanone,3-(4-methoxyphenyl)-3-(1-methyl-1H-indol-3-yl)-1-phenyl

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:5883-78-3 SDS

5883-78-3Downstream Products

5883-78-3Relevant academic research and scientific papers

Highly efficient heterobimetallic iron-magnesium-HMPA-catalyzed Michael-type Friedel-Crafts reactions of indoles and chalcones

Zhou, Wei,Li, Li,Xu, Li-Wen,Qiu, Hua-Yu,Lai, Guo-Qiao,Xia, Chun-Gu,Castanet, Anne-Sophie

, p. 1638 - 1645 (2008/09/20)

A simple and novel bimetallic catalyst, an iron and magnesium complex (Fe-Mg-hexamethylphosphoramide (HMPA)), with dual activation was found to be an effective and promising catalyst for the Michael-type Friedel-Crafts reactions of indoles with chalcones.

Chlorotrimethylsilane: A powerful Lewis acidic catalyst in Michael-type Friedel-Crafts reactions of indoles and enones

Xu, Li-Wen,Zhou, Wei,Yang, Lei,Xia, Chun-Gu

, p. 3095 - 3104 (2008/02/12)

Catalytic amount of chlorotrimethylsilane (TMSCl) was found to be an effective silicon Lewis acid catalyst in catalyzing the Michael-type Friedel-Crafts reactions of indoles and chalcones to afford corresponding 3-substituted indole derivatives in good to

A mild, efficient and improved protocol for the synthesis of novel indolyl crown ethers, di(indolyl)pyrazolyl methanes and 3-alkylated indoles using H 4[Si(W3O10)3]

Murugan, Rajendran,Karthikeyan, Murugesan,Perumal, Paramasivam T.,Reddy, Boreddy S.R.

, p. 12275 - 12281 (2007/10/03)

Efficient electrophilic substitution reactions of indoles with various aldehydes proceed smoothly in acetonitrile using heteropoly acid (H 4[Si(W3O10)3]) to afford the corresponding new indolyl crown ethers and

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