5405-90-3 Usage
Description
(2-methylcyclopentyl)cyclohexane is a chemical compound with the molecular formula C11H20. It is a saturated hydrocarbon belonging to the cycloalkanes family, which are cyclic hydrocarbons with single bonds. (2-methylcyclopentyl)cyclohexane consists of a cyclohexane ring and a methylcyclopentane ring connected to each other.
Uses
Used in Chemical Industry:
(2-methylcyclopentyl)cyclohexane is used as a solvent in various industrial and chemical processes for its low reactivity and ability to dissolve a wide range of substances.
Used in Pharmaceutical Synthesis:
(2-methylcyclopentyl)cyclohexane is used as a raw material in the synthesis of pharmaceuticals, contributing to the development of new medications.
Used in Agricultural Chemicals:
(2-methylcyclopentyl)cyclohexane is used as a raw material in the synthesis of agricultural chemicals, aiding in the production of effective crop protection agents.
Used in Organic Synthesis:
(2-methylcyclopentyl)cyclohexane is used as a building block in organic synthesis, enabling the creation of various organic compounds.
Used in Material Science:
(2-methylcyclopentyl)cyclohexane has potential applications in material science due to its unique structure and properties, which can be utilized to develop new materials with specific characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 5405-90-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,0 and 5 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5405-90:
(6*5)+(5*4)+(4*0)+(3*5)+(2*9)+(1*0)=83
83 % 10 = 3
So 5405-90-3 is a valid CAS Registry Number.
5405-90-3Relevant articles and documents
Carbazole hydrodenitrogenation over nickel phosphide and Ni-rich bimetallic phosphide catalysts
Bowker, Richard H.,Ilic, Boris,Carrillo, Bo A.,Reynolds, Michael A.,Murray, Brendan D.,Bussell, Mark E.
, p. 221 - 230 (2014/07/08)
Silica-supported nickel phosphide (Ni2P) and Ni-rich bimetallic phosphide catalysts were investigated for the hydrodenitrogenation (HDN) of carbazole with and without a benzothiophene co-feed. The Ni2P/ SiO2, Co0.1Ni1.9P/SiO2, and Fe 0.03Ni1.97P/SiO2 catalysts exhibited high carbazole HDN activities and out-performed a commercial sulfided Ni-Mo/Al 2O3 catalyst under the testing conditions employed. Co-feeding of benzothiophene inhibited carbazole HDN over the metal phosphides, but the Ni2P/SiO2 and Ni-rich bimetallic phosphide catalysts maintained higher activities than the sulfided Ni-Mo/Al 2O3 catalyst. The product selectivities of the metal phosphide and sulfide catalysts were similar, except that the sulfided Ni-Mo/Al2O3 catalyst yielded more hydrogenated carbazoles while the metal phosphide catalysts produced more of the partially hydrogenated hydrocarbon cyclohexylbenzene. The metal phosphide catalysts favored ring-opened (hexylcyclohexane) and ring-contracted ((2-methylcyclopentyl)cyclohexane) products, indicating the presence of metal and Br?nsted acid sites on the catalyst surfaces. The Ni2P/SiO2 and bimetallic phosphide catalysts exhibited excellent stabilities in the HDN conditions employed (carbazole-only and mixed feeds), as indicated by phase purity, average crystallite size and resistance to sulfur incorporation of the supported metal phosphide particles.
