59575-91-6 Usage
Uses
Used in Pharmaceutical Research:
Phenyl(2-pyridyl)methylamine hydrochloride is used as a research compound for the development of new pharmaceuticals. Its unique molecular structure allows for exploration in various therapeutic areas, including potential applications in drug discovery and synthesis.
Used in Medical Research:
In the field of medical research, Phenyl(2-pyridyl)methylamine hydrochloride is used as a biochemical reagent to study its interactions with biological systems. This can lead to a better understanding of its potential effects on human health and disease, as well as its possible use in diagnostic or therapeutic applications.
Used in Chemical Synthesis:
Phenyl(2-pyridyl)methylamine hydrochloride is used as a synthetic intermediate in the preparation of various chemical compounds. Its reactivity and structural features make it a valuable component in the synthesis of complex molecules, which can be further utilized in a wide range of applications, from pharmaceuticals to materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 59575-91-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,5,7 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 59575-91:
(7*5)+(6*9)+(5*5)+(4*7)+(3*5)+(2*9)+(1*1)=176
176 % 10 = 6
So 59575-91-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H12N2.ClH/c13-12(10-6-2-1-3-7-10)11-8-4-5-9-14-11;/h1-9,12H,13H2;1H
59575-91-6Relevant academic research and scientific papers
Carbon-carbon bond formations at the benzylic positions of N-benzylxanthone imines and N-benzyldi-1-naphthyl ketone imine
Niwa, Takashi,Suehiro, Takafumi,Yorimitsu, Hideki,Oshima, Koichiro
experimental part, p. 5125 - 5131 (2009/11/30)
Two N-benzyl imines are designed to allow for carbon-carbon bond formations at the aminated benzylic positions. Direct benzylic arylation reactions of N-benzylxanthone imine with aryl chlorides proceed under palladium catalysis in the presence of cesium hydroxide, yielding the corresponding benzhydrylamine derivatives. Alkylation reactions of N-benzyldi-1-naphthyl ketone imine with alkyl halides in the presence of potassium tert-butoxide afford the corresponding 1-phenylalkylamines in high yields. Conjugate addition of N-benzyldi-1-naphthyl ketone imine is also described.
Palladium-catalyzed benzylic arylation of N-benzylxanthone imine
Niwa, Takashi,Yorimitsu, Hideki,Oshima, Koichiro
supporting information; experimental part, p. 4689 - 4691 (2009/05/13)
(Chemical Equation Presented) The direct benzylic arylation of N-benzylxanthone imine with aryl chloride proceeds under palladium catalysis, yielding the corresponding coupling product. The product is readily transformed to benzhydrylamine. Taking into consideration that the imine is readily available from benzylic amine, the overall transformation represents a formal cross-coupling reaction of aryl halide with α-aminobenzyl metal.
