Welcome to LookChem.com Sign In|Join Free
  • or
3-methylcyclohex-4-ene-1,1,2,2-tetracarbonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13358-02-6

Post Buying Request

13358-02-6 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

13358-02-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13358-02-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,3,5 and 8 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 13358-02:
(7*1)+(6*3)+(5*3)+(4*5)+(3*8)+(2*0)+(1*2)=86
86 % 10 = 6
So 13358-02-6 is a valid CAS Registry Number.

13358-02-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methylcyclohex-4-ene-1,1,2,2-tetracarbonitrile

1.2 Other means of identification

Product number -
Other names 3-Methyl-4-cyclohexene-1,1,2,2-tetracarbonitrile

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:13358-02-6 SDS

13358-02-6Downstream Products

13358-02-6Relevant academic research and scientific papers

THE EFFECT OF THE STABILIZATION AND LOCALIZATION ENERGY ON THE REACTIVITY OF THE REAGENTS IN THE DIELS-ALDER REACTION

Konovalov, A. I.,Kiselev, V. D.

, p. 1018 - 1028 (2007/10/02)

The effect of the stabilization and localization energy on the reactivity of the addends in the Diels-Alder reaction was examined.The enthalpies of stabilization were calculated from data on the ionization potentials and electron affinities, and the chang

Reaktivity of Substituted 1,3-Butadienes in Diels-Alder-Reactions

Ruecker, Christa,Lang, Dietrich,Sauer, Juergen,Friege, Henning,Sustmann, Reiner

, p. 1663 - 1690 (2007/10/02)

Kinetic data for the reaction of substituted 1,3-dienes with tetracyanoethylene (TCNE) and other dienophiles are interpreted in terms of the FMO-model.While the expectations are fulfilled qualitatively, the kinetic data cannot be correlated quantitatively.This shows that in Diels-Alder reactions besides HOMO-LUMO separation other factors play an important role, for instance the 1,4-distance in the diene and the conformational equilibrium cisoid transoid of the diene.The kinetic data are in accord with a one-step mechanism of the cycloaddition reaction.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 13358-02-6