59575-91-6 Usage
General Description
Phenyl(2-pyridyl)methylamine hydrochloride is a biochemical reagent, often used in the area of pharmaceutical and medical research. This chemical compound belongs to the categories of pyridines, pharmacopoeia, and other related products. Its molecular structure consists of a pyridine ring attached to a phenyl group through a methylene bridge, providing diverse reactivity due to its aromatic and heterocyclic properties. As a hydrochloride, it is typically presented in a solid, crystalline form. As with many chemicals, it should be handled and stored with care to avoid unnecessary exposure or harm.
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 articles and documents
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.
