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1H-Indole, 2-methyl-1-[(4-methylphenyl)sulfonyl]-3-(1-phenylethenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

113685-34-0

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113685-34-0 Usage

Molecular Structure

2-methyl-1-[(4-methylphenyl)sulfonyl]-3-(1-phenylethenyl)-1H-indole consists of an indole ring with various substituents.

Indole ring

A bicyclic structure with a six-membered aromatic ring and a five-membered nitrogen-containing ring.

Methyl group at the 2-position

A CH3 group attached to the indole ring at the second position.

Sulfonyl group substituted on the 1-position

A (-SO2-) functional group connected to the indole ring at the first position, with a 4-methylphenyl moiety.

Ethenyl group attached to the 3-position

A vinyl-like (-CH=CH2) group connected to the indole ring at the third position.

Phenyl group connected to the ethenyl group

An aromatic ring with a delocalized pi system attached to the ethenyl group.

Chemical Class

The compound belongs to the class of organic compounds known as indoles and derivatives.

Indoles

A group of chemical compounds containing the indole ring structure.

Derivatives

Compounds with a modified indole structure, featuring additional functional groups or substituents.

Occurrence and Applications

Indoles and their derivatives are commonly found in natural products and have various pharmacological activities.

Natural products

Indoles can be found in a wide range of organisms, including plants, fungi, and bacteria.

Pharmacological activities

Indoles exhibit a diverse range of biological activities, such as antitumor, anti-inflammatory, and antimicrobial properties. They can also act as enzyme inhibitors or ligands for specific receptors.

Specific Properties and Reactivity

The properties and potential applications of 2-methyl-1-[(4-methylphenyl)sulfonyl]-3-(1-phenylethenyl)-1H-indole depend on its exact structure and the particular chemical reactions it undergoes.

Electronic properties

The presence of electron-donating and electron-withdrawing groups can influence the compound's reactivity and stability.

Steric properties

The size and shape of the substituents can affect the compound's reactivity, solubility, and interactions with other molecules.

Potential functionalization

The presence of reactive functional groups, such as the sulfonyl and ethenyl groups, allows for further chemical modifications and the synthesis of new derivatives with potentially useful properties.

Check Digit Verification of cas no

The CAS Registry Mumber 113685-34-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,6,8 and 5 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 113685-34:
(8*1)+(7*1)+(6*3)+(5*6)+(4*8)+(3*5)+(2*3)+(1*4)=120
120 % 10 = 0
So 113685-34-0 is a valid CAS Registry Number.

113685-34-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-1-(4-methylphenyl)sulfonyl-3-(1-phenylethenyl)indole

1.2 Other means of identification

Product number -
Other names 1H-Indole,2-methyl-1-[(4-methylphenyl)sulfonyl]-3-(1-phenylethenyl)

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:113685-34-0 SDS

113685-34-0Upstream product

113685-34-0Downstream Products

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