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Cyclodocosane, also known as dodecamantane or C12H24, is a cyclic alkane consisting of twelve carbon atoms arranged in a ring structure. It is a member of the cycloalkane family, which are saturated hydrocarbons with a closed carbon chain. Cyclodocosane is a colorless, odorless, and highly flammable liquid with a low melting point and boiling point. It is relatively stable and has limited reactivity due to its saturated nature. Cyclodocosane is primarily of academic interest and has no significant commercial applications, as it is challenging to synthesize and isolate in large quantities.

296-86-6

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296-86-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 296-86-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,9 and 6 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 296-86:
(5*2)+(4*9)+(3*6)+(2*8)+(1*6)=86
86 % 10 = 6
So 296-86-6 is a valid CAS Registry Number.

296-86-6SDS

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 cyclodocosane

1.2 Other means of identification

Product number -
Other names Cyclodokosan

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:296-86-6 SDS

296-86-6Downstream Products

296-86-6Relevant academic research and scientific papers

Cyclooctane metathesis catalyzed by silica-supported tungsten pentamethyl [(ΞSiO)W(Me)5]: Distribution of macrocyclic alkanes

Riache, Nassima,Callens, Emmanuel,Samantaray, Manoja K.,Kharbatia, Najeh M.,Atiqullah, Muhammad,Basset, Jean-Marie

supporting information, p. 15089 - 15094 (2015/02/19)

Metathesis of cyclic alkanes catalyzed by the new surface complex [(ΞSiO)W(Me)5] affords a wide distribution of cyclic and macrocyclic alkanes. The major products with the formula CnH2n are the result of either a ring contraction or ring expans

Conformation of the Cycloalkanes C14H28, C16H32, and C22H44 in the Liquid and High-Temperature Crystalline Phases by Vibrational Spectroscopy

Shannon, V. L.,Strauss, H. L.,Snyder, R. G.,Elliger, C. A.,Mattice, W. L.

, p. 1947 - 1958 (2007/10/02)

This paper reports a conformational analysis, by means of vibrational red spectroscopy, of the conformationally disorded phases of c-C14H28, c-C16H32, and c-C22H44.From the observed spectra, the concentration of the lowest energy conformer in the liquid state has been estimated along with the concentration ratios of certain short sequences of trans and gauche bonds.The experimentally derived values of the concentrations are compared with calculated values derived from various sets of conformers whose calculated strain energies have been previously reported in the literature.Good agreement was found for c-C14H28.However, for c-C16H32, the calculated concentration of the lowest energy conformer is significantly higher than is found experimentally and, in addition, there are some serious differences between the observed and calculated values of the concentrations of the conformational sequences.The most important factor contributing to the discrepanciens between the measured and calculated conformational statistics is probably the force field used in the strain energy calculations.For c-C22H44, a relatively flexible ring, the experimentally measured concentrations are in reasonable agreement with values derived from a set of diamond-lattice conformers.The distribution of conformers in the high-temperature crystalline phase of all three cycloalkanes is similar to, but somewhat narrower than, that found for the liquid.In the case of c-C14H28, for which a measurement is possible, the concentration of the lowest energy (rectangular) conformer in the high-temperature crystalline phase is estimated to be about 70 +/- percent, a value somewhat higher than the 60 +/- 10percent estimated for the liquid.For c-C22H44, the concentration of gauche bonds is used to characterize the liquid and the high-temperature crystalline phases.In terms of the average number of gauche bonds per ring, the high-temperature phase of c-C22H44 is found to lie closer to the liquid than to the low-temperature phase.

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