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Bicyclo[4.2.1]nonane is a cyclic hydrocarbon compound with the molecular formula C9H16. It consists of two fused cyclohexane rings, with one carbon atom shared between them, forming a nine-membered ring structure. Bicyclo[4.2.1]nonane is an example of a bridged bicyclic system, where the bridge is a single carbon atom connecting two carbons of the cyclohexane rings. Bicyclo[4.2.1]nonane is a structural isomer of other nonane derivatives and is known for its unique strain and stability due to the fusion of the two rings. It is an important intermediate in organic synthesis and can be used in the preparation of various pharmaceuticals and other chemical compounds.

284-10-6

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284-10-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 284-10-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,8 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 284-10:
(5*2)+(4*8)+(3*4)+(2*1)+(1*0)=56
56 % 10 = 6
So 284-10-6 is a valid CAS Registry Number.

284-10-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name bicyclo[4.2.1]nonane

1.2 Other means of identification

Product number -
Other names bicyclo<4.2.1>nonan

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:284-10-6 SDS

284-10-6Downstream Products

284-10-6Relevant academic research and scientific papers

Formation of Bicyclooctane, Bicyclononane, and Bicyclononane by Transannular Radical Cyclisations

MacCorquodale, Finlay,Walton, John C.

, p. 1456 - 1457 (1987)

Cyclohept-4-enylmethyl radicals undergo transannular cyclisation to give bicyclooctane; likewise, bicyclononane and bicyclononane are obtained from cyclo-oct-4-enylmethyl radicals.

Cyclisation of 5-Bromomethyl-cycloheptene and -cyclo-octene: a New Route to Bicyclooctanes and Bicyclononanes

MacCorquodale, Finlay,Walton, John C.

, p. 347 - 352 (2007/10/02)

Reduction of 5-(bromomethyl)cycloheptene with tributyltin hydride gave bicyclooctane; similar reduction of 5-(bromomethyl)cyclo-octene gave bicyclononane together with some bicyclononane.The cyclohept-4-enylmethyl radical intermediate

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