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3-Phenylhexahydro-1H-oxazolo[3,4-a]pyridine is a complex organic compound with the molecular formula C12H16N2O. It is a heterocyclic compound, featuring a six-membered nitrogen-containing ring (oxazolopyridine) fused to a six-membered carbon ring. The phenyl group is attached to the third carbon of the hexahydro ring, which is a saturated ring structure. 3-phenylhexahydro-1H-oxazolo[3,4-a]pyridine is of interest in medicinal chemistry and may have potential applications in the development of pharmaceuticals due to its unique structure and the ability to form various interactions with biological targets. Its synthesis and properties are subjects of research in the field of organic chemistry, with potential implications for drug design and the creation of new therapeutic agents.

2563-84-0

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2563-84-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2563-84-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,6 and 3 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2563-84:
(6*2)+(5*5)+(4*6)+(3*3)+(2*8)+(1*4)=90
90 % 10 = 0
So 2563-84-0 is a valid CAS Registry Number.

2563-84-0Relevant academic research and scientific papers

Pyrolysis of perhydro[1,2-c][1,3]oxazines: A green method of synthesizing 2,3-dehydropiperidine enamines

Cook, A. Gilbert,Schering, Christine A.,Campbell, Pauline A.,Hayes, Samantha S.

, p. 5451 - 5454 (2005)

Heat pyrolysis of the oxazines formed from 2-piperidineethanol produced 2,3-dehydropiperidine enamines. The same results were observed when these oxazines were irradiated with microwaves. Various 2-substituted perhydrooxazines were synthesized by allowing 2-piperidineethanol or 2-piperidinemethanol to react with aldehydes or ketones.

Electrooxidative cyclization of hydroxyamino compounds possessing a benzyl group

Okimoto, Mitsuhiro,Ohashi, Kousuke,Yamamori, Haruki,Nishikawa, Shinnosuke,Hoshi, Masayuki,Yoshida, Takashi

, p. 1315 - 1322 (2012/06/30)

Several novel 2-aryl-1,3-oxazinane and 2-aryl-1,3-oxazolidine derivatives were synthesized from N-benzyl-2-piperidineethanols and N-benzyl-2- piperidinemethanols, respectively, by using electrooxidative methods in methanol. For these reactions, the yields of the corresponding cyclized compounds were significantly increased by using catalytic amounts of iodide ions. In contrast, 3-dialkylamino-1-phenylpropanols afforded the expected cyclic 6-phenyl-1,3-oxazinane derivatives using only a small excess of base. Georg Thieme Verlag Stuttgart · New York.

Novel application of electrooxidative method for the cyclization of N-benzyl-2-(hydroxymethyl)-and N-benzyl-2-(2-hydroxyethyl)piperidines

Okimoto, Mitsuhiro,Yoshida, Takashi,Hoshi, Masayuki,Ohashi, Kousuke

, p. 2471 - 2478 (2011/04/26)

Several novel 1,3-oxazinane and oxazolidine derivatives were obtained from the corresponding N-benzyl-2-(2-hydroxyethyl)-and N-benzyl-2-(hydroxymethyl) piperidines via electrochemical oxidation. The reactions were carried out in methanol under basic conditions. The yields of the cyclic products were significantly improved using catalytic amounts of iodide ions, which presumably act as effective electron carriers in the two-electron oxidation process. The Japan Institute of Heterocyclic Chemistry.

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