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

75032-40-5

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75032-40-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75032-40-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,0,3 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 75032-40:
(7*7)+(6*5)+(5*0)+(4*3)+(3*2)+(2*4)+(1*0)=105
105 % 10 = 5
So 75032-40-5 is a valid CAS Registry Number.

75032-40-5SDS

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-but-3-enyl-2-methyl-1-phenyl-1H-indene

1.2 Other means of identification

Product number -
Other names -

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:75032-40-5 SDS

75032-40-5Relevant academic research and scientific papers

Intramolecular Ring Closure Reactions of Cyclopropene Derivatives as a Method for Synthesizing Novel Tricyclic Ring Compounds

Padwa, Albert,Rieker, William F.,Rosenthal, Robert J.

, p. 1353 - 1360 (2007/10/02)

The thermal and photosensitized reactions of several 4-(methyldiphenylcyclopropenyl)-1-butenes have been studied.The thermolysis of these systems gave substituted tricyclo2,7>heptanes in good yield.The formation of this ring system invo

Photosensitized Electron-Transfer-Induced Reactions of Some Cyclopropene Derivatives

Padwa, Albert,Chou, Chuen S.,Rieker, William F.

, p. 4555 - 4564 (2007/10/02)

The 9,10-dicyanoanthracene-sensitized rearrangement of several 3-phenyl-substituted cyclopropenes to indenes in acetonitrile has been studied. When an unsymmetrically 1-phenyl-2-methyl-substituted cyclopropene was used, the major indene obtained correspon

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