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2-Chlorobicyclo[2.2.2]oct-5-ene-2-carbonitrile is a chemical compound with the molecular formula C9H8ClN. It is a halogenated derivative of bicyclo[2.2.2]oct-5-ene-2-carbonitrile, featuring a chlorine atom attached to the bicyclic ring structure and a nitrile group (CN) at the 2-position. 2-chlorobicyclo[2.2.2]oct-5-ene-2-carbonitrile is characterized by its unique molecular geometry and reactivity, which can be influenced by the presence of the chlorine atom and the nitrile group. It may be used in organic synthesis as a building block for more complex molecules, particularly in the pharmaceutical and chemical industries. Due to its potential reactivity and the presence of a halogen, it is important to handle 2-chlorobicyclo[2.2.2]oct-5-ene-2-carbonitrile with care, following appropriate safety protocols.

6962-73-8

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6962-73-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6962-73-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,6 and 2 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6962-73:
(6*6)+(5*9)+(4*6)+(3*2)+(2*7)+(1*3)=128
128 % 10 = 8
So 6962-73-8 is a valid CAS Registry Number.

6962-73-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-chlorobicyclo[2.2.2]oct-2-ene-5-carbonitrile

1.2 Other means of identification

Product number -
Other names 5-chloro-5-cyanobicyclo<2.2.2>oct-2-ene

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:6962-73-8 SDS

6962-73-8Relevant academic research and scientific papers

LOW-MOLECULAR COMPOUND, POLYMER, MATERIAL FOR ELECTRONIC DEVICES, COMPOSITION FOR ELECTRONIC DEVICES, ORGANIC ELECTROLUMINESCENT ELEMENT, ORGANIC SOLAR CELL ELEMENT, DISPLAY AND LIGHTING EQUIPMENT

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Page/Page column 66, (2012/09/21)

A subject for the invention is to provide compounds where a film formation can be made by a wet film formation method, a heating temperature at the film formation is low, the film formed therefrom has high stability, and the other layers can be laminated thereon by a wet film formation method or another method. The compounds are usable as a material for electronic device which decreases little in charge transport efficiency or luminescent efficiency and which have excellent driving stability. The invention resides in a compound and a polymer which are characterized by having a elimination group of a specific structure and in an organic compound characterized by having a elimination group having a low elimination temperature.

NICOTINIC RECEPTOR NON-COMPETITIVE ANTAGONISTS

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, (2011/12/14)

The present invention relates to compounds that modulate nicotinic receptors as non-competitive antagonists, methods for their synthesis, methods for use, and their pharmaceutical compositions.

NOVEL FUSED BRIDGED BICYCLIC HETEROARYL SUBSTITUTED 6-ALKYLIDENE PENEMS AS POTENT BETA-LACTAMASE INHIBITORS

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, (2011/12/12)

A compound of formula (I) or formula (Ia) Wherein R1 , Ra, R2, X, R3 , Y1, y2, A, B and C are as defined herein. Also, pharmaceutical compositions comprising such compounds and excipients, methods of treating bacterial infections comprising administering such compounds, methods for making such compounds and hydrates of such compounds.

Synthesis of an Alleged Constituent of New Brunswick Cranberry Leaves: The So-Called Cannivonine

Kozikowski, Alan P.,Schmiesing, Richard J.

, p. 1000 - 1007 (2007/10/02)

An unambiguous ten-step synthesis of the compound possessing the reputed structure of the cranberry alkaloid cannivonine (1) is presented.Stereoselective reductive amination of the known cis-Δ5,6-2-octalone, protection of the nitrogen substitue

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