38473-30-2 Usage
Description
N-Hydroxyphentermine is a metabolite of Phentermine, an anorexic and controlled substance classified as a stimulant. It is derived from the Amphetamine family of compounds. This substance is known for its potential effects on the central nervous system, which may contribute to its various applications.
Uses
Used in Pharmaceutical Industry:
N-Hydroxyphentermine is used as an active pharmaceutical ingredient for its stimulant properties, which can help in the treatment of conditions related to appetite suppression and weight management. Its anorexic effects make it a potential candidate for pharmaceutical formulations aimed at addressing obesity and related health issues.
Used in Research and Development:
In the field of scientific research, N-Hydroxyphentermine can be utilized as a compound for studying the effects of stimulants on the central nervous system. This can contribute to the development of new drugs and therapies for various neurological and psychiatric disorders.
Used in Drug Metabolism Studies:
As a metabolite of Phentermine, N-Hydroxyphentermine can be used in drug metabolism studies to understand the biotransformation processes in the body. This knowledge can help in the design of more effective and safer medications with reduced side effects.
Check Digit Verification of cas no
The CAS Registry Mumber 38473-30-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,4,7 and 3 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 38473-30:
(7*3)+(6*8)+(5*4)+(4*7)+(3*3)+(2*3)+(1*0)=132
132 % 10 = 2
So 38473-30-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H15NO/c1-10(2,11-12)8-9-6-4-3-5-7-9/h3-7,11-12H,8H2,1-2H3
38473-30-2Relevant articles and documents
Electrochemical Reduction of Tertiary Nitroalkanes to Amines
Ohmori, Hidenobu,Furusako, Shoji,Kashu, Mieko,Ueda, Chihiro,Masui, Masaichiro
, p. 3345 - 3353 (2007/10/02)
Electrochemical reduction of tertiary nitroalkanes, 2-substituted-1,1-dimethyl-1-nitroethanes (1), was investigated in aqueous buffer solutions.In polarography, 1 with a phenyl group and/or a hydroxyl group at the 2-position showed an ill-defined wave in the weakly acidic and neutral pH region at relatively high negative potentials, in addition to a well-defined wave arising from the reduction of 1 to the corresponding hydroxylamine (2).Controlled potential electrolysis of 1 at the potential of the former wave gave the 1,1-dimethylethylamines (3) as well as the hydroxylamines 2.The amines 3 are formed exclusively from 2, probably via the O-protonated form.It is suggested that a phenyl group at the 2-position facilitates the reduction of 2 to 3 by enhancing the adsorption of 2 at the mercury cathode and that a hydroxyl group, while it interferes with the adsorption, assists the reduction by intramolecular hydrogen-bonding to stabilize the O-protonated form of 2.Keywords - tertiary nitroalkane; alkylhydroxylamine; electrochemical reduction; polarography; controlled potential electrolysis.