1357289-10-1

Basic information

• Product Name: C₂₁H₂₂N₂O₆
• Synonyms: C₂₁H₂₂N₂O₆
• CAS NO: 1357289-10-1
• Molecular Weight: 398.415
• Mol File: 1357289-10-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₂₁H₂₂N₂O₆(CAS DataBase Reference)
• NIST Chemistry Reference: C₂₁H₂₂N₂O₆(1357289-10-1)
• EPA Substance Registry System: C₂₁H₂₂N₂O₆(1357289-10-1)

Safety Data

• Hazardous Substances Data: 1357289-10-1(Hazardous Substances Data)

Upstream product

• 1246616-66-9 dimethyl 3-(benzyloxy)-4-oxo-4H-pyran-2,5-dicarboxylate 
• 61477-40-5 (R)-3-amino-1-butanol 
• 1246617-67-3 C₁₈H₁₇NO₇ 
• 1246616-65-8 methyl 4-benzyloxy-2-((dimethylamino)methylene)acetoacetate 
• 32807-28-6 Methyl 4-chloroacetoacetate 
• 100-51-6 benzyl alcohol 
• 82961-76-0 4-benzyloxy-3-oxobutyric acid methyl ester 
• 1357289-08-7 2,5-dimethyl 3-(benzyloxy)-1-(2,2-dimethoxyethyl)-4-oxo-1,4-dihydropyridine-2,5-dicarboxylate 

Downstream Products

• 1206102-11-5 (4R,12aS)-7-(benzyloxy)-N-(2,4-difluorobenzyl)-4-methyl-6,8-dioxo-3,4,6,8,12,12a-hexahydro-2H-pyrido[1′,2’:4,5]-pyrazino[2,1-b][1,3]oxazine-9-carboxamide 

Relevant articles and documents

PROCESS FOR PREPARING COMPOUND HAVING HIV INTEGRASE INHIBITORY ACTIVITY

A process for preparing a compound represented by formula (Y1) or (Y2) [wherein Rx is an optionally substituted carbocyclyl lower alkyl, or the like] or a salt thereof, using a novel process for preparing a pyridone derivative represented by formula (X4) [wherein R1d is hydrogen, halogen, or the like; R2d is hydrogen, a lower alkyl optionally substituted with substituent E, or the like; R4d is a lower alkyl optionally substituted with substituent E, or the like; and R6d is a lower alkyl group optionally substituted with substituent group E, or the like].