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1-Phenyl-2-(2-piperidin-1-yl-ethoxy)-ethanol is a complex organic compound with the molecular formula C17H25NO2. It is a derivative of phenylethanol, featuring a phenyl group (C6H5) attached to the first carbon atom, and a 2-piperidin-1-yl-ethoxy group attached to the second carbon atom. The piperidin-1-yl-ethoxy group consists of a piperidine ring (a saturated six-membered nitrogen-containing ring) connected to an ethoxy group (C2H5O). 1-phenyl-2-(2-piperidin-1-yl-ethoxy)-ethanol is known for its potential applications in the pharmaceutical industry, particularly as a precursor in the synthesis of various drugs and medicinal compounds. Its unique structure allows for a range of chemical reactions and interactions, making it a valuable component in the development of new therapeutic agents.

787-85-9

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787-85-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 787-85-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,8 and 7 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 787-85:
(5*7)+(4*8)+(3*7)+(2*8)+(1*5)=109
109 % 10 = 9
So 787-85-9 is a valid CAS Registry Number.

787-85-9Downstream Products

787-85-9Relevant academic research and scientific papers

Studies on cognitive enhancing agents. II. Antiamnestic and antihypoxic activities of 1-aryl-2-(2-aminoethoxy)ethanols

Ono,Yamafuji,Chaki,Morita,Todo,Maekawa,Kitamura,Tai,Narita

, p. 1488 - 1491 (2007/10/03)

A series of 2-(2-aminoethoxy)-1-phenylethanols having a variety of N- and phenyl-substitution patterns as well as 5- and 6-membered heteroaryl counterparts of our prototype compound 1 (2-(2-dimethylaminoethoxy)-1- phenylethanol) have been prepared and evaluated for antiamnestic and antihypoxic activities. Compound 3b, the 3-methylphenyl analogue of 1, proved to be significantly more potent than I in reversing electroconvulsive shock- induced amnesia as well as CO2-induced learning-impairment in mice. It exhibited low acute toxicity in mice and afforded a greater brain/serum concentration ratio than 1 after oral administration to rats.

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