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Bicyclo[3.3.2]decane is a cyclic hydrocarbon compound with the molecular formula C10H18. It features a unique bicyclic structure, consisting of two fused six-membered rings, with one carbon atom shared between them. This molecule is known for its high strain due to the presence of two quaternary carbon atoms and a trans-decalin ring fusion, which results in a non-planar, twisted conformation. Bicyclo[3.3.2]decane is an important structural motif in various natural products and pharmaceuticals, and it serves as a precursor in the synthesis of complex organic compounds. Its chemical properties and reactivity are influenced by the strain in the molecule, making it a subject of interest in organic chemistry research.

283-50-1

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283-50-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 283-50-1 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, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 283-50:
(5*2)+(4*8)+(3*3)+(2*5)+(1*0)=61
61 % 10 = 1
So 283-50-1 is a valid CAS Registry Number.

283-50-1SDS

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[3.3.2]decane

1.2 Other means of identification

Product number -
Other names Bicyclo<3,3,2>decan

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:283-50-1 SDS

283-50-1Downstream Products

283-50-1Relevant academic research and scientific papers

Diademane and Structurally Related Compounds, II. Catalytic Rearrangements and Hydrogenations

Kaufmann, Dieter,Schallner, Otto,Meyer, Lueder-Ulrich,Fick, Hans-Heinrich,Meijere, Armin de

, p. 1377 - 1385 (2007/10/02)

Copper, silver, gold, and rhodium compounds catalyze the rearrangement of diademane (1) to triquinacene (5) and snoutene (7), respectively.Known mechanism may be adopted to explain this behaviour.The catalytic hydrogenation of 1 leads to a mixture of 6 products, 9 - 14, the composition of which was independent of the extent of reaction.Adamantane, the thermodynamically most stable isomer of all conceivable "hexahydrodiademanes", was not detected.

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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