29215-00-7 Usage
Description
N,N-Dimethyl-2-[(o-methyl-α-phenylbenzyl)oxy]ethanamine N-oxide, also known as a metabolite of Orphenadrine, is a pale yellow solid with unique chemical properties. It is derived from the metabolism of Orphenadrine, a drug used to treat various muscle movement disorders. N,N-Dimethyl-2-[(o-methyl-α-phenylbenzyl)oxy]ethanamine N-oxide exhibits a distinct chemical structure that contributes to its potential applications in different industries.
Uses
Used in Pharmaceutical Industry:
N,N-Dimethyl-2-[(o-methyl-α-phenylbenzyl)oxy]ethanamine N-oxide is used as an intermediate compound for the synthesis of various pharmaceutical products. Its unique chemical structure allows it to be a key component in the development of new drugs targeting muscle movement disorders and other related conditions.
Used in Research and Development:
In the field of research and development, N,N-Dimethyl-2-[(o-methyl-α-phenylbenzyl)oxy]ethanamine N-oxide serves as a valuable compound for studying the metabolic pathways of Orphenadrine and other related drugs. This understanding can lead to the discovery of new drug candidates and improved treatment options for patients suffering from muscle movement disorders.
Used in Quality Control and Analysis:
N,N-Dimethyl-2-[(o-methyl-α-phenylbenzyl)oxy]ethanamine N-oxide is also utilized in quality control and analytical processes to ensure the purity and efficacy of Orphenadrine and its related drug products. By analyzing the presence and concentration of this metabolite, researchers and quality control professionals can assess the quality and consistency of the drug products in the market.
Used in Drug Metabolism Studies:
N,N-Dimethyl-2-[(o-methyl-α-phenylbenzyl)oxy]ethanamine N-oxide is used as a reference compound in drug metabolism studies. Understanding how this metabolite is produced and processed in the body can provide insights into the metabolism of Orphenadrine and other similar drugs, potentially leading to the development of more effective and safer medications.
Check Digit Verification of cas no
The CAS Registry Mumber 29215-00-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,2,1 and 5 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 29215-00:
(7*2)+(6*9)+(5*2)+(4*1)+(3*5)+(2*0)+(1*0)=97
97 % 10 = 7
So 29215-00-7 is a valid CAS Registry Number.
InChI:InChI=1/C18H23NO2/c1-15-9-7-8-12-17(15)18(16-10-5-4-6-11-16)21-14-13-19(2,3)20/h4-12,18H,13-14H2,1-3H3
29215-00-7Relevant articles and documents
A chemoselective deoxygenation of N-oxides by sodium borohydride-Raney nickel in water
Gowda, Narendra B.,Rao, Gopal Krishna,Ramakrishna, Ramesha A.
supporting information; experimental part, p. 5690 - 5693 (2010/11/05)
A simple and convenient protocol for deoxygenation of aliphatic and aromatic N-oxides to the corresponding amines in good to excellent yield using sodium borohydride-Raney nickel in water is reported. Other functional moieties such as alkenes, halides, ethers, and amides are unaffected under the present reaction condition.
The effect of alkyl substitution in drugs. XXI. Synthesis and a comparative pharmacological study of a number of potential orphenadrine metabolites.
den Besten,Mulder,Funcke,Nauta
, p. 538 - 542 (2007/10/05)
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