362489-59-6

Basic information

• Product Name: 1-tert-butyl 3-methyl 4-{[(1R)-1-phenylethyl]amino}-5,6-dihydropyridine-1,3(2H)-dicarboxylate
• Synonyms: 1-tert-butyl 3-methyl 4-{[(1R)-1-phenylethyl]amino}-5,6-dihydropyridine-1,3(2H)-dicarboxylate
• CAS NO: 362489-59-6
• Molecular Weight: 360.453
• Mol File: 362489-59-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-tert-butyl 3-methyl 4-{[(1R)-1-phenylethyl]amino}-5,6-dihydropyridine-1,3(2H)-dicarboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: 1-tert-butyl 3-methyl 4-{[(1R)-1-phenylethyl]amino}-5,6-dihydropyridine-1,3(2H)-dicarboxylate(362489-59-6)
• EPA Substance Registry System: 1-tert-butyl 3-methyl 4-{[(1R)-1-phenylethyl]amino}-5,6-dihydropyridine-1,3(2H)-dicarboxylate(362489-59-6)

Safety Data

• Hazardous Substances Data: 362489-59-6(Hazardous Substances Data)

Upstream product

• 3886-69-9 (R)-1-phenyl-ethyl-amine 
• 220389-30-0 1-tert-butyl 3-methyl 4-hydroxy-5,6-dihydropyridine-1,3(2H)-dicarboxylate 
• 24424-99-5 di-tert-butyl dicarbonate 
• 161491-24-3 methyl 1-tert-butoxycarbonyl-4-oxo-3-piperidinecarboxylate 

Downstream Products

• 362489-60-9 1-tert-butyl 3-methyl (3S,4R)-4-{[(1R)-1-phenylethyl]-amino}piperidine-1,3-dicarboxylate 
• 388109-62-4 1-tert-butyl 3-methyl (3R,4R)-4-{[(1R)-1-phenylethyl]-amino}piperidine-1,3-dicarboxylate 
• 1207065-50-6 1-tert-butyl 3-methyl (3R,4S)-4-{[(1R)-1-phenylethyl]-amino}piperidine-1,3-dicarboxylate 
• 1207065-51-7 1-tert-butyl 3-methyl (3S,4S)-4-{[(1R)-1-phenylethyl]-amino}piperidine-1,3-dicarboxylate 
• 503167-62-2 4-((R)-1-phenyl-ethylamino)-piperidine-1,3-dicarboxylic acid 1-tert-butyl ester 3-methyl ester 

Relevant articles and documents

Efficient and practical asymmetric synthesis of 1-tert-butyl 3-methyl (3R,4R)-4-(2-oxo-2,3-dihydro-1H-benzimidazol-1-yl)piperidine-1,3-dicarboxylate, a useful intermediate for the synthesis of nociceptin antagonists

An efficient and practical asymmetric synthesis of 1-tert-butyl 3-methyl (3R,4R)-4-(2-oxo-2,3-dihydro-1H-benzimidazol-1-yl)piperidine-1,3-dicarboxylate 1, a useful intermediate for the synthesis of nociceptin antagonists, has been developed. This method i

N-ureidoheterocycloalkyl-piperidines as modulators of chemokine receptor activity

The present application describes modulators of CCR3 of formula (I): or pharmaceutically acceptable salt forms thereof, useful for the prevention of asthma and other allergic diseases.