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Octylcyclopentane is an organic compound with the molecular formula C13H26. It is a cyclic alkane, consisting of a cyclopentane ring with an octyl chain attached to it. This hydrocarbon is a colorless liquid with a low melting point and boiling point, and it is insoluble in water but soluble in organic solvents. Octylcyclopentane is primarily used as a solvent, a chemical intermediate in the synthesis of various compounds, and as a component in the formulation of specialty chemicals. Due to its unique structure, it exhibits specific properties that make it suitable for certain applications in the chemical industry.

1795-20-6

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1795-20-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1795-20-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,9 and 5 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1795-20:
(6*1)+(5*7)+(4*9)+(3*5)+(2*2)+(1*0)=96
96 % 10 = 6
So 1795-20-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H26/c1-2-3-4-5-6-7-10-13-11-8-9-12-13/h13H,2-12H2,1H3

1795-20-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name octylcyclopentane

1.2 Other means of identification

Product number -
Other names n-Octylcyclopentane

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:1795-20-6 SDS

1795-20-6Downstream Products

1795-20-6Relevant academic research and scientific papers

From Dimethylamine to Pyrrolidine: The Development of an Improved Nickel Pincer Complex for Cross-Coupling of Nonactivated Secondary Alkyl Halides

Perez Garcia, Pablo M.,Di Franco, Thomas,Epenoy, Alexandre,Scopelliti, Rosario,Hu, Xile

, p. 258 - 261 (2016/01/12)

Replacement of a dimethyl amino group of the amidobis(amine) nickel(II) pincer complex (1), [(MeN2N)Ni-Cl], by a pyrrolidino group resulted in a new nickel(II) pincer complex (2), [(PyrNMeNN)Ni-Cl]. Complex 2 is an efficient catalyst for Kumada and Suzuki-Miyaura cross-coupling of nonactivated secondary alkyl halides, while complex 1 is largely inactive. The significant activity difference is tentatively attributed to a minimal structural difference, which leads to a more hemilabile ligand.

Thermal Addition of Alkanes to Alkenes. V. Addition of Cyclohexane to 1-Octene in a Free Radical Chain reaction at Supercritical Fluid Conditions

Metzger, Juergen O.

, p. 767 - 781 (2007/10/02)

Alkanes can be added to alkenes in a thermally initiated free radical chain reaction ("ane reaction").Kinetic and mechanistic studies on the addition of cyclohexane (1) to 1-octene (2) (molar ratio = 100:1) at 330-450 deg C and pressures of up to 300 bar

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