898820-42-3

Basic information

• Product Name: 2-(N-tert-butoxycarbonylamino)-5-phenylpyridine
• Synonyms: 2-(N-tert-butoxycarbonylamino)-5-phenylpyridine
• CAS NO: 898820-42-3
• Molecular Weight: 270.331
• Mol File: 898820-42-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-(N-tert-butoxycarbonylamino)-5-phenylpyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(N-tert-butoxycarbonylamino)-5-phenylpyridine(898820-42-3)
• EPA Substance Registry System: 2-(N-tert-butoxycarbonylamino)-5-phenylpyridine(898820-42-3)

Safety Data

• Hazardous Substances Data: 898820-42-3(Hazardous Substances Data)

Upstream product

• 36016-38-3 tert-Butyl N-hydroxycarbamate 
• 1008-88-4 3-phenylpyridine 
• 33421-40-8 5-phenyl-pyridin-2-ylamine 
• 24424-99-5 di-tert-butyl dicarbonate 
• 159451-66-8 tert-butyl N-(5-bromopyridin-2-yl)carbamate 
• 98-80-6 phenylboronic acid 

Relevant articles and documents

Azonia Aromatic Cations by Ring-Closing Metathesis: Synthesis of Azaquinolizinium Cations

A strategy based on a ring-closing metathesis (RCM) reaction of pyridinium azadienes in the presence of the second generation Grubbs catalyst was employed as a new approach to synthesize the 1-azaquinolizinium (pyrido[1,2-a]pyrimidin-5-ium) heterocycle and some simple derivatives. This method was also successfully applied to the first reported synthesis of the benzo-1-azaquinolizinium (pyrimido[2,1-a]isoquinolinium) cation by using the Hoveyda-Grubbs catalyst in Cl2CHCHCl2 at 130 C.

Bicyclic heterocycles as cannabinoid receptor modulators

The present application describes compounds according to Formula I, pharmaceutical compositions comprising at least one compound according to Formula I and optionally one or more additional therapeutic agents and methods of treatment using the compounds according to Formula I both alone and in combination with one or more additional therapeutic agents. The compounds have the general Formula I: including all prodrugs, pharmaceutically acceptable salts and stereoisomers, R1, R2, R3, R3a, R4, A, B, n, Y and Z are described herein.