1357622-86-6

Basic information

• Product Name: C₂₅H₃₅BrN₂O₆
• Synonyms: C₂₅H₃₅BrN₂O₆
• CAS NO: 1357622-86-6
• Molecular Weight: 539.467
• Mol File: 1357622-86-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₂₅H₃₅BrN₂O₆(CAS DataBase Reference)
• NIST Chemistry Reference: C₂₅H₃₅BrN₂O₆(1357622-86-6)
• EPA Substance Registry System: C₂₅H₃₅BrN₂O₆(1357622-86-6)

Safety Data

• Hazardous Substances Data: 1357622-86-6(Hazardous Substances Data)

Upstream product

• 55904-12-6 ((4R,5S)-5-Hydroxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-methanol 
• 1357623-31-4 C₇H₁₁N₃O₃ 
• 1357622-26-4 (R,E)-2-(3-bromophenoxy)methyl-5-methylhex-3-enyl acetate 
• 1357622-27-5 (R)-3-acetoxy-2-((3-bromophenoxy)methyl)propanol 
• 1357622-28-6 (R)-1-acetoxy-3-azido-2-((3-bromophenoxy)methyl)propane 
• 1357622-29-7 (S)-3-azido-2-((3-bromophenoxy)methyl)propanol 
• 1357622-30-0 (R)-1-azido-3-(tert-butyl)dimethylsilyloxy-2-((3-bromophenoxy)methyl)propane 
• 1357622-34-4 (R)-1-amino-3-(tert-butyl)dimethylsilyloxy-2-((3-bromophenoxy)methyl)propane 
• 1357622-36-6 (R)-1-(tert-butyl)dimethylsilyloxy-2-((3-bromophenoxy)methyl)-3-formylaminopropane 
• 1357622-38-8 (R)-1-(tert-butyl)dimethylsilyloxy-2-((3-bromophenoxy)methyl)-3-isocyanopropane 
• 1357622-52-6 ((4R,5S)-5-(azidomethyl)-2,2-dimethyl-1,3-dioxolan-4-yl)methyl acetate 
• 1357622-55-9 C₇H₁₃N₃O₃ 
• 1357622-64-0 C₃₁H₄₉BrN₂O₆Si 
• 1357623-20-1 C₁₃H₁₇BrO₆S 

Relevant articles and documents

Diversity oriented and chemoenzymatic synthesis of densely functionalized pyrrolidines through a highly diastereoselective Ugi multicomponent reaction

A highly diastereoselective Ugi reaction involving a chiral cyclic imine, two enantiomerically pure isocyanides and various carboxylic acids was employed for the synthesis of polyfunctionalized pyrrolidines. Both chiral substrates have been efficiently prepared by chemoenzymatic methodologies from readily available achiral substrates. This highly convergent approach can find an application in the fragment-based drug discovery process. The Royal Society of Chemistry 2012.