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

89619-41-0

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89619-41-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89619-41-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,6,1 and 9 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 89619-41:
(7*8)+(6*9)+(5*6)+(4*1)+(3*9)+(2*4)+(1*1)=180
180 % 10 = 0
So 89619-41-0 is a valid CAS Registry Number.

89619-41-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ethyl-1-phenyl-1H-indene

1.2 Other means of identification

Product number -
Other names 1H-Indene,2-ethyl-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:89619-41-0 SDS

89619-41-0Upstream product

89619-41-0Relevant academic research and scientific papers

Ruthenium-catalyzed cyclization of alkyne-epoxide functionalities through alternation of the substituent and structural skeleton of epoxides

Ming-Yuan, Lin,Madhushaw, Reniguntala J.,Liu, Rai-Shung

, p. 7700 - 7704 (2007/10/03)

Treatment of 1-(o-ethynylphenyl)-2-alkyl-2-aryl epoxides with TpRuPPh 3(CH3CN)2PF6 catalyst (10 mol %) in hot toluene (100 °C, 12 h) led to an atypical cyclization and gave 1-aryl-2-alkyl-1H-indene derivatives a

Ozonolysis of a Series of 1-Substituted Indenes. The Substituent Steric Effects on Ozonide Exo/Endo Ratios

Miura, Masahiro,Nojima, Masatomo,Kusabayashi, Shigekazu,McCullough, Kevin J.

, p. 2932 - 2936 (2007/10/02)

The ozonolysis of a series of disubstituted (1,2 and 1,3) and trisubstituted (1,2,3) indenes 1-28 in carbon tetrachloride at 20 deg C has been investigated.The major product in each case was the corresponding bicyclic ozonide, usually obtained as a mixtur

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