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1H-Indene, 1-ethyl-2,3-dihydro-2-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88534-46-7

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88534-46-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88534-46-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,5,3 and 4 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 88534-46:
(7*8)+(6*8)+(5*5)+(4*3)+(3*4)+(2*4)+(1*6)=167
167 % 10 = 7
So 88534-46-7 is a valid CAS Registry Number.

88534-46-7SDS

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-ethyl-2-methyl-2,3-dihydro-1H-indene

1.2 Other means of identification

Product number -
Other names 1-Ethyl-2-methylindan

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:88534-46-7 SDS

88534-46-7Upstream product

88534-46-7Downstream Products

88534-46-7Relevant academic research and scientific papers

Acid-catalyzed Reactions of Aromatic Hydrocarbons with Alkanes and Cycloalkanes. X. Alkylations with Cyclohexane

Miethchen, Ralf,Steege, Sigrid,Kroeger, Carl-Friedrich

, p. 823 - 834 (2007/10/02)

The complex reaction mixtures of the nonconventional alkylation of benzene with cyclohexane in the presence of Lewis/proton acids and promotors were investigated by gas-liquid chromatography and mass spectrometry.Four representative groups of hydrocarbons were found including cycloalkylbenzenes, substituted indanes or tetralines (C12H16), C1-C6-alkylbenzenes and isomeric biscycloalkyls (C12H22).Their formation is interpreted as a competition between alkylation, (without or with isomerization), ringfission with cycloalkylation or fragmentation, and self-alkylation; phenylcycloalkylcations and phenylalkylcations are the intermediates.

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