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14112-41-5

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14112-41-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14112-41-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,1,1 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 14112-41:
(7*1)+(6*4)+(5*1)+(4*1)+(3*2)+(2*4)+(1*1)=55
55 % 10 = 5
So 14112-41-5 is a valid CAS Registry Number.

14112-41-5Relevant articles and documents

Aminomethylation of 2-cyclopentylidene-cyclopentanone

Roth,Thassler

, p. 900 - 906 (1971)

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Synthesis of renewable high-density fuels using cyclopentanone derived from lignocellulose

Yang, Jinfan,Li, Ning,Li, Guangyi,Wang, Wentao,Wang, Aiqin,Wang, Xiaodong,Cong, Yu,Zhang, Tao

, p. 2572 - 2574 (2014)

By the combination of solvent-free aldol condensation and one-step hydrodeoxygenation under mild reaction conditions, a high-density (0.866 g mL-1) bicyclic C10 hydrocarbon was synthesized in high overall yield (up to 80%) using cyclopentanone derived from lignocellulose. The Royal Society of Chemistry 2014.

Direct conversion of carboxylic acids (Cn) to alkenes (C2n - 1) over titanium oxide in absence of noble metals

Oliver-Tomas, Borja,Renz, Michael,Corma, Avelino

, p. 1 - 8 (2016/02/05)

Carbon-carbon bond formations and deoxygenation reactions are important for biomass up-grading. The classical ketonic decarboxylation of carboxylic acids provides symmetrical ketones with 2n + 1 carbon atoms and eliminates three oxygen atoms. Herein, this reaction is carried out with titanium oxide at 400°C, and an olefin with 2n + 1 carbon atoms is obtained instead of the ketone. For olefin formation hydrogen transfer reactions are required from suitable precursors to form aromatics and coke. Additional aldol condensation reactions increase further molecular weight in the product mixture. Hence, a combination of titanium oxide with a hydrodeoxygenation bed provides double amount of diesel fuel as the combination with zirconium oxide when reacting hexose-derived pentanoic acid.

Reductive dimerization and oligomerization of alcohols, ketones, and aldehydes to hydrocarbons on a promoted, fused iron catalyst

Glebov,Zaikin,Mikaya,Kliger

, p. 296 - 308 (2014/08/05)

A new reductive dimerization and oligomerization reaction of (C5 and C6) cycloalkanols and cycloalkanones, benzaldehyde, and benzyl alcohol to hydrocarbons containing as many, or more, carbon atoms as the reactant oxygenated compound on a promoted, fused iron catalyst proceeds at a temperature of 250-350°C, a hydrogen pressure of 0.1-1 MPa, a specific feed rate of oxygenated reagent of 80-320 g h-1kg-1Ct, and a hydrogen space velocity of 1 × 103 to 20 × 103 h-1. Possible reaction mechanisms have been considered.

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