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80025-16-7

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80025-16-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80025-16-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,0,2 and 5 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 80025-16:
(7*8)+(6*0)+(5*0)+(4*2)+(3*5)+(2*1)+(1*6)=87
87 % 10 = 7
So 80025-16-7 is a valid CAS Registry Number.

80025-16-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,7-Bismethylen-1,4-cyclooctadien

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:80025-16-7 SDS

80025-16-7Upstream product

80025-16-7Downstream Products

80025-16-7Relevant articles and documents

Alkynes and Cumulenes, XIV. - Thermal and Photochemical Dimerization of 1,2,4-Pentatriene (Vinylallene)

Schneider, Ralf,Siegel, Herbert,Hopf, Henning

, p. 1812 - 1825 (2007/10/02)

On heating at 170 degC in the gas phase 1,2,4-pentatriene (1) dimerizes to the six-membered hydrocarbons 2, 5, and 13, to the eight-membered ring hydrocarbons 8 and 18 as well as to the tetrahydronaphthalene 16; in a side reaction 1 cycloisomerizes to 3-methylene-1-cyclobutene (11).The C10H12-hydrocarbons are very likely produced via diradical intermediates, only 2, 5, and 13 being primary products.On the other hand, for the dimers 8, 16, and 18 reasonable electrocyclic reaction paths may be postulated.The sensitized photodimerization of 1 leads to the cyclobutane derivatives 31, 33, 35 and to 28 as a thermally produced secondary product from 33.The exclusive cyclobutane formation suggests that 1 behaves analogously to 1,3-butadiene in sensitized photodimerizations.

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