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1,4-Cyclohexadiene, 1,2-diethyl-4,5-dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87226-82-2

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87226-82-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87226-82-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,2,2 and 6 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 87226-82:
(7*8)+(6*7)+(5*2)+(4*2)+(3*6)+(2*8)+(1*2)=152
152 % 10 = 2
So 87226-82-2 is a valid CAS Registry Number.

87226-82-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-diethyl-4,5-dimethylcyclohexa-1,4-diene

1.2 Other means of identification

Product number -
Other names 1,4-Cyclohexadiene,1,2-diethyl-4,5-dimethyl

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:87226-82-2 SDS

87226-82-2Downstream Products

87226-82-2Relevant academic research and scientific papers

Transannular [4 + 2] Cycloaddition Reactions of Cobalt-Complexed Macrocyclic Dienynes

Karabiyikoglu, Sedef,Merlic, Craig A.

supporting information, p. 4086 - 4089 (2015/09/01)

The first transannular [4 + 2] cycloaddition reactions of macrocyclic dicobalt hexacarbonyl-dienyne complexes were demonstrated. Complexes were conveniently prepared through palladium(II)-catalyzed intramolecular oxidative cyclization of bis(vinylboronate esters) followed by complexation with dicobalt octacarbonyl. Transannular [4 + 2] cycloaddition reactions of the complexes occurred at lower temperatures and shorter times than transannular Diels-Alder reactions of metal-free dienynes. Intermolecular control reactions confirmed the effect of cobalt complexation on [4 + 2] cycloaddition reactions of unactivated alkynes and dienes.

An efficient cobalt catalyst for the neutral Diels-Alder reaction of acyclic 1,3-dienes with internal alkynes

Hilt, Gerhard,Korn, Tobias J.

, p. 2783 - 2785 (2007/10/03)

The efficiently cobalt(I)-catalysed neutral Diels-Alder type reactions of internal alkynes with substituted 1,3-dienes is described. The regiochemistry for the dihydroaromatic products of reactions of isoprene with unsymmetrical reaction partners (2-alkyn

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