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2-[(4-Methylphenyl)sulfanyl]indane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

93435-72-4

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93435-72-4 Usage

Type of compound

Sulfur-containing organic compound

Classification

Indane derivatives

Usage

Synthesis of pharmaceuticals and agrochemicals

Odor

Characteristic odor

Solubility

Insoluble in water, soluble in organic solvents (e.g., ethanol, acetone)

Biological activities

Exhibits potential biological activities

Therapeutic applications

Studied for its potential therapeutic applications

Check Digit Verification of cas no

The CAS Registry Mumber 93435-72-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,4,3 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 93435-72:
(7*9)+(6*3)+(5*4)+(4*3)+(3*5)+(2*7)+(1*2)=144
144 % 10 = 4
So 93435-72-4 is a valid CAS Registry Number.
InChI:InChI=1/C16H16S/c1-12-6-8-15(9-7-12)17-16-10-13-4-2-3-5-14(13)11-16/h2-9,16H,10-11H2,1H3

93435-72-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-methylphenyl)sulfanyl-2,3-dihydro-1H-indene

1.2 Other means of identification

Product number -
Other names 2-[(4-Methylphenyl)sulfanyl]indane

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:93435-72-4 SDS

93435-72-4Relevant academic research and scientific papers

Iodine-catalyzed addition of aromatic mercaptans to indene

Pudukulathan, Zubaidha K.,Kasa, Anjaneyulu

experimental part, p. 187 - 195 (2012/06/01)

Molecular iodine catalysis of additions of various substituted thiophenols to indene to afford the corresponding sulfides in good yields under mild conditions is reported. The regioselectivity of addition can be fine-tuned by modifying the reaction condit

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