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5-Hexenyl, 2,2-dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

71880-21-2

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71880-21-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71880-21-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,8,8 and 0 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 71880-21:
(7*7)+(6*1)+(5*8)+(4*8)+(3*0)+(2*2)+(1*1)=132
132 % 10 = 2
So 71880-21-2 is a valid CAS Registry Number.

71880-21-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-Dimethyl-hex-5-enyl-Radikal

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:71880-21-2 SDS

71880-21-2Downstream Products

71880-21-2Relevant academic research and scientific papers

Homogeneous Rate Constants for Coupling between Electrochemically Generated Aromatic Anion Radicals and Alkyl Radicals

Pedersen, Steen U.,Lund, Torben

, p. 397 - 402 (2007/10/02)

Rate constants have been measured for the coupling between hexenyl radicals and 2,2-dimethylhexenyl radicals and electrogenerated anion radicals of anthracene, 9,10-diphenylanthracene, benzophenone and quinoxaline.The rate constant for all four reactions in N,N-dimethylformamide is log k2 = 9.1(5), which is in accordance previous results in 1,2-dimethoxyethane for naphthalene and benzophenone anion radicals and 1-hexenyl radicals.The data indicate that the redox potential of the aromatic anion radical has only a minor influence on the rate of coupling with alkyl radicals.The rate constants for anion radicals of 9,10-diphenylanthracene and benzophenone were somewhat lower, 6(1) x 108 M-1 s-1, which for 9,10-diphenylanthracene might be caused by steric hindrance by the two phenyl groups.The conclusion is that the coupling reaction between aromatic anion radicals and alkyl radicals has all the characteristics of a radical-radical coupling.

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