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280-65-9

280-65-9

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280-65-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 280-65-9 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 0 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 280-65:
(5*2)+(4*8)+(3*0)+(2*6)+(1*5)=59
59 % 10 = 9
So 280-65-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H16/c1-3-8-5-2-6-9(4-1)7-8/h8-9H,1-7H2

280-65-9SDS

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 bicyclo[3.3.1]nonane

1.2 Other means of identification

Product number -
Other names Bicyclo[3.3.1]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:280-65-9 SDS

280-65-9Relevant articles and documents

-

Sasaki,T. et al.

, p. 2230 - 2234 (1973)

-

Conformational studies by dynamic NMR. 76.1 stereodynamics of ring inversion of bicyclo[3.3.1]nonan-9-one

Grilli, Stefano,Lunazzi, Lodovico,Mazzanti, Andrea

, p. 3563 - 3565 (2000)

-

Chemoselectivity of Nitroxylation of Cage Hydrocarbons

Ivleva, E. A.,Klimochkin, Yu. N.,Leonova, M. V.

, p. 1702 - 1710 (2020/12/01)

Abstract: The composition of reaction mixtures obtained by nitroxylation of 13 cage hydrocarbons with 100% nitric acid and its mixtures with acetic acid, acetic anhydride, and methylene chloride has been studied. More reactive substrates react with lowest

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

MacCorquodale, Finlay,Walton, John C.

, p. 1456 - 1457 (2007/10/02)

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

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