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Spiro[5.5]undeca-1,4-diene, 3-ethylidene- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87482-34-6

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87482-34-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87482-34-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,4,8 and 2 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 87482-34:
(7*8)+(6*7)+(5*4)+(4*8)+(3*2)+(2*3)+(1*4)=166
166 % 10 = 6
So 87482-34-6 is a valid CAS Registry Number.

87482-34-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-ethylidenespiro[5.5]undeca-1,4-diene

1.2 Other means of identification

Product number -
Other names 3-ethylidenespiro<5,5>undeca-1,4-diene

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:87482-34-6 SDS

87482-34-6Relevant academic research and scientific papers

FLASH VACUUM THERMOLYSIS OF DISPIROALKADIENES

Kraakmann, P. A.,Nibbering, E. T. J.,Wolf, W. H. de,Bickelhaupt, F.

, p. 5109 - 5124 (1987)

The Flash Vacuum Thermolysis (FVT) of dispirotetradeca -4,13-diene (7a). dispirotrideca-4,12-diene (7b) and dispirodeca-4,9-diene (7e) at 500-750 deg C is reported.The complicated reaction mixture from 7a and 7b (Scheme 3) included at lower temperatures vinylspiroalkadienes 9, ethylidenespiroalkadiene 10b, β-ethylcycloalkabenzenes 11, while at higher temperatures, p-n-alkyl-(5) and p-sec-alkylstyrenes 14 and p-divinylbenzene (15) dominated.Product formation is explained by invoking diradicals 8,6 and 12 as well as the cyclophanes 1 and 13 as intermediates.For 7e, the product mixture was less complicated and consisted of p-ethylstyrene (5e), 15 and, unexpectedly,p-isopropylstyrene (14e) which contains one carbon more than the starting material.The analysis and interpretation of product formation largely confirms previously suggested reaction pathways and furnishes further interesting details.However, new and unexpected features are also encountered, especially in the fragmentations of 1 and 13 which may stimulate future investigations on the thermal behaviour of these relatively simple hydrocarbons.

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