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Bicyclo[3.2.2]nonane is a cyclic alkane with the molecular formula C9H16. It consists of two fused cyclohexane rings, forming a nonane backbone with three carbon atoms bridging the two rings. This unique structure results in a highly strained molecule due to the presence of two quaternary carbon centers and the overall compact shape. Bicyclo[3.2.2]nonane is an important compound in organic chemistry, as it serves as a precursor to various synthetic reactions and can be used to study the effects of ring strain on chemical reactivity. Its properties, such as boiling point, melting point, and solubility, are influenced by its strained structure, making it an interesting subject for research in the field of organic chemistry.

283-19-2

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283-19-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 283-19-2 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 3 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 283-19:
(5*2)+(4*8)+(3*3)+(2*1)+(1*9)=62
62 % 10 = 2
So 283-19-2 is a valid CAS Registry Number.

283-19-2SDS

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[3.2.2]nonane

1.2 Other means of identification

Product number -
Other names bicyclo[3.2.2]-nonane

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:283-19-2 SDS

283-19-2Downstream Products

283-19-2Relevant academic research and scientific papers

Organic Peroxides, XIV. The Thermal Decomposition of Polycyclic tert-Butyl Bridgehead Peroxycarboxylates

Ruechardt, Christoph,Golzke, Volker,Range, Guenter

, p. 2769 - 2785 (2007/10/02)

Eleven bridgehead peresters (1, 2, 5 - 8, 10, 12, 14, 18, 21) have been prepared for the first time and the products and the kinetics of their thermal decomposition were investigated.The correlations of all known thermolysis constants of bridgehead peresters with the steric substituent constants φf, with the solvolysis constants of the corresponding bridgehead bromides, as well as with the change in strain enthalpy ΔHsp for hydride abstraction from the bridgehead, as calculated by the procedure of v.R.Schleyer, were analysed.The thermolysis constants of these peresters are mainly determined by the polar effect in the transition state of the perester fragmentation.

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