402933-56-6

Basic information

• Product Name: tert-Butyl [6-(2-hydroxyethyl)pyridin-2-yl]carbamate
• Synonyms: 2-Amino-6-(2-hydroxyethyl)pyridine, 2-BOC protected;tert-Butyl [6-(2-hydroxyethyl)pyridin-2-yl]carbamate;tert-Butyl [6-(2-hydroxyethyl)pyridin-2-yl]carbamate, 2-[(tert-Butoxycarbonyl)amino]-6-(2-hydroxyethyl)pyridine
• CAS NO: 402933-56-6
• Molecular Formula: C₁₂H₁₈N₂O₃
• Molecular Weight: 238.28292
• Mol File: 402933-56-6.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: tert-Butyl [6-(2-hydroxyethyl)pyridin-2-yl]carbamate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-Butyl [6-(2-hydroxyethyl)pyridin-2-yl]carbamate(402933-56-6)
• EPA Substance Registry System: tert-Butyl [6-(2-hydroxyethyl)pyridin-2-yl]carbamate(402933-56-6)

Safety Data

• Hazardous Substances Data: 402933-56-6(Hazardous Substances Data)

Upstream product

• 52085-14-0 4-benzoxy-salicylaldehyde 
• 68-12-2 N,N-dimethyl-formamide 
• 90101-22-7 2-(tert-butoxycarbonylamino)-6-picoline 
• 24424-99-5 di-tert-butyl dicarbonate 
• 408365-87-7 ethyl 2-(6-((tert-butoxycarbonyl)amino)pyridin-2-yl)acetate 
• 1824-81-3 2-Amino-6-methylpyridine 

Downstream Products

• 408365-88-8 2-{6-[(tert-butoxycarbonyl)amino]-2-pyridinyl}ethyl 4-methylbenzenesulfonate 

Relevant articles and documents

Synthesis and structure–activity relationship of 2,6-disubstituted pyridine derivatives as inhibitors of β-amyloid-42 aggregation

It is assumed that amyloid-β aggregation is a crucial event in the pathogenesis of Alzheimer's disease. Novel 2,6-disubstituted pyridine derivatives were designed to interact with the β-sheet conformation of Aβ via donor–acceptor–donor hydrogen bond forma

Gem-substituted αvβ3 antagonists

The present invention relates to a class of compounds represented by the Formula I. or a pharmaceutically acceptable salt thereof, pharmaceutical compositions comprising compounds of the Formula I, and methods of selectively inhibiting or antagonizing the αVβ3and/or the αVβ5integrin.