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1,1,4,6-Tetramethylindane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

941-60-6

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941-60-6 Usage

Physical state

Colorless liquid

Chemical class

Organic compound

Specific type

Indan

Primary use

Fragrance ingredient in cosmetic products

Additional use

Production of perfumes and scented products

Odor

Pleasant

Industrial application

Solvent in various processes

Health hazard

Skin irritation

Health hazard

Eye irritation

Exposure

Should be limited and strictly controlled

Industry focus

Fragrance industry

Management

Potential industrial and health concerns need careful management

Check Digit Verification of cas no

The CAS Registry Mumber 941-60-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,4 and 1 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 941-60:
(5*9)+(4*4)+(3*1)+(2*6)+(1*0)=76
76 % 10 = 6
So 941-60-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H18/c1-9-7-10(2)11-5-6-13(3,4)12(11)8-9/h7-8H,5-6H2,1-4H3

941-60-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3,5,6-tetramethyl-1,2-dihydroindene

1.2 Other means of identification

Product number -
Other names 1,1,4,6-Tetramethyl-indan

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:941-60-6 SDS

941-60-6Downstream Products

941-60-6Relevant academic research and scientific papers

A copper(II) triflate-catalyzed tandem friedel-crafts alkylation/ cyclization process towards dihydroindenes

Zhang, Yugen,Chen, Liwei,Lu, Ting

supporting information; experimental part, p. 1055 - 1060 (2011/07/09)

A one-pot synthesis of dihydroindenes from substituted benzenes and haloalkenes was developed. The reaction proceeded via a copper(II) triflate [Cu(OTf)2]-catalyzed tandem Friedel-Crafts alkylation/cyclization process with high efficiency under

Diaminoindane derivatives

-

, (2008/06/13)

The invention relates to diaminoindane derivatives represented by the following formula: STR1 wherein R1 and R2 are each selected from the group consisting of a hydrogen atom and a lower alkyl group having from 1 to 4 carbon atoms, and a process for preparing same.

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