15995-50-3 Usage
General Description
N-Phenyl-2-aminonorbornane is a complex organic compound that belongs to the category of organic compounds known as analgesics and has been used historically for pain relief. Known to be slightly soluble in water, it is potentially used in medical or scientific research due to its structural similarity to several types of amphetamines. Its core structure, a norbornane backbone, with a phenyl group and an amino group attached, makes it a derivative of norbornane. N-Phenyl-2-aminonorbornane is characterized by a two-ring structure with seven carbon atoms and twelve hydrogen atoms. Please note that detailed properties such as stability, toxicity or potential applications need further authoritative references.
Check Digit Verification of cas no
The CAS Registry Mumber 15995-50-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,9,9 and 5 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 15995-50:
(7*1)+(6*5)+(5*9)+(4*9)+(3*5)+(2*5)+(1*0)=143
143 % 10 = 3
So 15995-50-3 is a valid CAS Registry Number.
15995-50-3Relevant articles and documents
Gasc et al.
, p. 1943,1948 (1978)
An unusual peroxide-mediated amination of cycloalkanes with nitroarenes
Deng, Guojun,Chen, Wenwen,Li, Chao-Jun
supporting information; experimental part, p. 353 - 356 (2009/10/25)
A direct amination of simple cycloalkanes with nitroarenes mediated by peroxides has been discovered. Various secondary arylamines were obtained efficiently from cycloalkanes. The reaction tolerates a wide range of functionalities as well as aqueous condi
Intermolecular hydroamination and hydroarylation reactions of alkenes in ionic liquids
Lapis, Alexandre A.M.,DaSilveira Neto, Brenno A.,Scholten, Jackson D.,Nachtigall, Fabiane M.,Eberlin, Marcos N.,Dupont, Jairton
, p. 6775 - 6779 (2007/10/03)
Intermolecular hydroamination or hydroarylation reactions of norbornene and cyclohexadiene performed with catalytic amounts of Br?nsted or Lewis acid in ionic liquids were found to provide higher selectivity and yields than those performed in classical organic solvents. The ionic liquid increases the acidity of the media and stabilizes ionic intermediates through the formation of supramolecular aggregates.
