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Bicyclo[3.2.2]non-8-ene-6,6,7,7-tetracarbonitrile is a complex organic compound with the molecular formula C13H8N4. It features a bicyclic structure with a nine-membered ring and a double bond in the 8th position. The compound has four nitrile groups (-CN) attached to the carbon atoms at positions 6, 6, 7, and 7. This unique structure gives it potential applications in various chemical reactions and synthesis processes. Due to its stability and reactivity, it can be used as a building block for the creation of more complex molecules and compounds. The compound's properties, such as its melting point, boiling point, and solubility, can be influenced by the presence of the nitrile groups and the bicyclic structure, making it an interesting subject for further research and development in the field of organic chemistry.

6342-44-5

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6342-44-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6342-44-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,4 and 2 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6342-44:
(6*6)+(5*3)+(4*4)+(3*2)+(2*4)+(1*4)=85
85 % 10 = 5
So 6342-44-5 is a valid CAS Registry Number.

6342-44-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name bicyclo[3.2.2]non-8-ene-6,6,7,7-tetracarbonitrile

1.2 Other means of identification

Product number -
Other names Bicyclo[3.2.2]non-8-en-6,6,7,7-tetracarbonitril

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:6342-44-5 SDS

6342-44-5Downstream Products

6342-44-5Relevant academic research and scientific papers

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.

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