50385-28-9 Usage
Description
2-(2-pyridin-2-ylethyl)aniline is an organic compound characterized by a chemical formula of C13H13N2. It features a benzene ring with an aniline group (C6H5NH2) and a pyridine ring, which are connected by a two-carbon bridge. 2-(2-pyridin-2-ylethyl)aniline is known for its structural and reactive properties, making it a versatile intermediate in the synthesis of pharmaceuticals and organic dyes.
Uses
Used in Pharmaceutical Industry:
2-(2-pyridin-2-ylethyl)aniline serves as an intermediate in the synthesis of various drugs, including anti-cancer and anti-inflammatory medications. Its unique structure and reactivity contribute to the development of these pharmaceuticals.
Used in Neurological Disorders Treatment:
2-(2-pyridin-2-ylethyl)aniline is considered a potential target for the treatment of neurological disorders due to its ability to interact with neurotransmitter receptors in the brain, offering a promising avenue for therapeutic intervention.
Used in Material Science and Engineering:
2-(2-pyridin-2-ylethyl)aniline has been utilized in the preparation of functionalized polymers, which have applications in material science and engineering, enhancing the properties of various materials for diverse uses.
Check Digit Verification of cas no
The CAS Registry Mumber 50385-28-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,3,8 and 5 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 50385-28:
(7*5)+(6*0)+(5*3)+(4*8)+(3*5)+(2*2)+(1*8)=109
109 % 10 = 9
So 50385-28-9 is a valid CAS Registry Number.
InChI:InChI=1/C13H14N2/c14-13-7-2-1-5-11(13)8-9-12-6-3-4-10-15-12/h1-7,10H,8-9,14H2
50385-28-9Relevant articles and documents
Substituted piperidines
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, (2008/06/13)
The compounds are of the heterocyclic class of 2-phenethylpiperidines having an amido substituent in the ortho position of the phenethyl moiety. Substituents in the ortho position include formamido, benzamido, cinnamamido, 2-thiophenecarboxamido, alkanesulfonamido and alkanoylamido. They are useful as antiarrhythmic and/or antiserotonin agents. The novel compounds are prepared by reaction of appropriately substituted o-aminophenethylpiperidines and the carbonyl or sulfonyl halides or anhydrides. Typical embodiments of this invention are 4-methoxy-2'-[2-(1-methyl-2-piperidyl)ethyl]benzanilide and 2'-[2-(1-methyl-2-piperidyl)ethyl]cinnamanilide.
