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N-4-Piperidinyl-4-piperidinamine, also known as tetrapropylammonium perruthenate (TPAP), is a chemical compound with the molecular formula C10H24N3. It is a powerful oxidizing agent and is commonly used in organic chemistry as a catalyst for the selective oxidation of primary and secondary alcohols to aldehydes and ketones. TPAP is a stable, crystalline white powder that is air-stable and soluble in organic solvents such as acetone and dichloromethane. It has become a popular reagent in chemical synthesis due to its efficiency and relatively mild reaction conditions, making it a valuable tool for producing a variety of valuable chemical products.

508201-22-7

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508201-22-7 Usage

Uses

Used in Pharmaceutical Industry:
N-4-Piperidinyl-4-piperidinamine is used as a catalyst for the selective oxidation of primary and secondary alcohols to aldehydes and ketones, which is crucial in the synthesis of complex organic molecules and pharmaceutical compounds.
Used in Fine Chemical Industry:
N-4-Piperidinyl-4-piperidinamine is used as a catalyst in the production of fine chemicals, where selective oxidation is required to obtain specific chemical products.
Used in Academic Research Laboratories:
N-4-Piperidinyl-4-piperidinamine is used as a reagent in academic research for the synthesis of complex organic molecules, providing a mild and efficient method for selective oxidation of alcohols.

Check Digit Verification of cas no

The CAS Registry Mumber 508201-22-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,8,2,0 and 1 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 508201-22:
(8*5)+(7*0)+(6*8)+(5*2)+(4*0)+(3*1)+(2*2)+(1*2)=107
107 % 10 = 7
So 508201-22-7 is a valid CAS Registry Number.

508201-22-7Upstream product

508201-22-7Downstream Products

508201-22-7Relevant academic research and scientific papers

The effect of substitution on the utility of piperidines and octahydroindoles for reversible hydrogen storage

Cui, Yi,Kwok, Samantha,Bucholtz, Andrew,Davis, Boyd,Whitney, Ralph A.,Jessop, Philip G.

, p. 1027 - 1037 (2008/12/20)

Substituted piperidines and octahydroindoles are compared in terms of their usability as reversible organic hydrogen storage liquids for hydrogen-powered fuel cells. Theoretical Gaussian calculations indicate which structural features are likely to lower the enthalpy of dehydrogenation. Experimental results show that attaching electron donating or conjugated substituents to the piperidine ring greatly increases the rate of catalytic dehydrogenation, with the greatest rates being observed with 4-aminopiperidine and piperidine-4-carboxamide. Undesired side reactions were observed with some compounds such as alkyl transfer reactions during the dehydrogenation of 4-dimethylaminopiperidine, C-O and C-N cleavage reactions during hydrogenation and/or subsequent dehydrogenation of 4-alkoxy and 4-amino indoles, and disproportionation during the hydrogenation of 4-aminopyridine. The Royal Society of Chemistry and the Centre National de la Recherche Scientifique.

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