1185730-50-0

Basic information

• Product Name: methyl 6-((3-(4,5-dimethoxy-2-nitrophenyl)-3-hydroxypropyl)(methyl)amino)-6-oxohexanoate
• Synonyms: methyl 6-((3-(4,5-dimethoxy-2-nitrophenyl)-3-hydroxypropyl)(methyl)amino)-6-oxohexanoate
• CAS NO: 1185730-50-0
• Molecular Weight: 412.44
• Mol File: 1185730-50-0.mol

Chemical Properties

• CAS DataBase Reference: methyl 6-((3-(4,5-dimethoxy-2-nitrophenyl)-3-hydroxypropyl)(methyl)amino)-6-oxohexanoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 6-((3-(4,5-dimethoxy-2-nitrophenyl)-3-hydroxypropyl)(methyl)amino)-6-oxohexanoate(1185730-50-0)
• EPA Substance Registry System: methyl 6-((3-(4,5-dimethoxy-2-nitrophenyl)-3-hydroxypropyl)(methyl)amino)-6-oxohexanoate(1185730-50-0)

Safety Data

• Hazardous Substances Data: 1185730-50-0(Hazardous Substances Data)

Upstream product

• 956139-36-9 3-(4,5-dimethoxy-2-nitrophenyl)-3-hydroxypropyl 4-methylbenzenesulfonate 
• 35444-44-1 methyl adipoyl chloride 
• 956139-39-2 C₁₂H₁₈N₂O₅ 
• 956139-40-5 1-(4,5-dimethoxy-2-nitrophenyl)-3-methylaminopropan-1-ol tosylate salt 

Downstream Products

• 1185730-61-3 C₂₃H₃₀N₄O₉ 
• 1402555-57-0 2,5-dioxopyrrolidin-1-yl 1-chloro-9-(4,5-dimethoxy-2-nitrophenyl)-12-methyl-2,7,13-trioxo-8-oxa-3,6,12-triazaoctadecan-18-oate 
• 1402555-55-8 methyl 1-chloro-9-(4,5-dimethoxy-2-nitrophenyl)-12-methyl-2,7,13-trioxo-8-oxa-3,6,12-triazaoctadecan-18-oate 
• 1426822-47-0 C₂₂H₃₄N₄O₉ 
• 1402555-56-9 1-chloro-9-(4,5-dimethoxy-2-nitrophenyl)-12-methyl-2,7,13-trioxo-8-oxa-3,6,12-triazaocta-triazaoctadecan-18-oic acid 
• 1185730-49-7 2,5-dioxopyrrolidin-1-yl 14-(4,5-dimethoxy-2-nitrophenyl)-17-methyl-5,12,18-trioxo-13-oxa-4,11,17-triazatricos-1-yn-23-oate 
• 1185730-63-5 C₂₈H₄₀N₄O₁₀ 
• 1185730-51-1 methyl 14-(4,5-dimethoxy-2-nitrophenyl)-17-methyl-5,12,18-trioxo-13-oxa-4,11,17-triazatricos-1-yn-23-oate 

Relevant articles and documents

Cyclic caged morpholinos: Conformationally gated probes of embryonic gene function

Feeling a bit cagey: Morpholino-based antisense reagents have been caged through oligonucleotide cyclization (see scheme), enabling photocontrol of gene expression in zebrafish embryos and larvae. Using these reagents, the timing of exocrine cell fate commitment in the developing pancreas has been examined. Copyright

Photocleavable linker methods and compositions

Bifunctional linkers are provided that comprise a photocleavable moiety flanked by two different amine reactive moieties. In some embodiments the photocleavable moiety is a dimethoxynitrobenzyl moiety. In other embodiments the photocleavable moiety is 8-b

Versatile synthesis and rational design of caged morpholinos

Embryogenesis is regulated by genetic programs that are dynamically executed in a stereotypic manner, and deciphering these molecular mechanisms requires the ability to control embryonic gene function with similar spatial and temporal precision. Chemical