719303-10-3

Basic information

• Product Name: 2-hydroxymethyl-4-methoxy-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-carbaldehyde O-[3-(tert-butyl-diphenyl-silanyloxy)-4-fluoro-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-2-ylmethyl]-oxime
• CAS NO: 719303-10-3
• Molecular Weight: 779.895
• Mol File: 719303-10-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-hydroxymethyl-4-methoxy-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-carbaldehyde O-[3-(tert-butyl-diphenyl-silanyloxy)-4-fluoro-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-2-ylmethyl]-oxime(CAS DataBase Reference)
• NIST Chemistry Reference: 2-hydroxymethyl-4-methoxy-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-carbaldehyde O-[3-(tert-butyl-diphenyl-silanyloxy)-4-fluoro-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-2-ylmethyl]-oxime(719303-10-3)
• EPA Substance Registry System: 2-hydroxymethyl-4-methoxy-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-carbaldehyde O-[3-(tert-butyl-diphenyl-silanyloxy)-4-fluoro-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-2-ylmethyl]-oxime(719303-10-3)

Safety Data

• Hazardous Substances Data: 719303-10-3(Hazardous Substances Data)

Upstream product

• 719302-84-8 5'-O-amino-3'-O-tert-butyldiphenylsilyl-2'-fluorothymidine 
• 171176-06-0 5'-O-phthalimido-2'-fluorothymidine 
• 318246-97-8 5'-O-(4,4'-dimethoxytrityl)-2'-O-methyl-3'-deoxy-3'-C-styryl-5-methyluridine 
• 198703-60-5 5'-O-(4,4'-dimethoxytrityl)-2'-O-methyl-3'-deoxy-3'-C-formyl-5-methyluridine 
• 153631-19-7 5'-O-(4,4'-dimethoxytrityl)-2'-O-methyl-5-methyluridine 
• 122799-38-6 1-(2'-deoxy-2'-fluoro-β-D-ribofuranosyl)-5-methyluracil 
• 719302-94-0 5'-O-(4,4'-dimethoxytrityl)-3'-O-(4-methylphenoxy)thiocarbonyl-2'-O-methyl-5-methyluridine 

Downstream Products

• 719302-99-5 C₄₄H₅₀FN₅O₁₂ 

Relevant articles and documents

Synthesis of 2′-Substituted MMI Linked Nucleosidic Dimers: An Optimization Study in Search of High Affinity Oligonucleotides for Use in Antisense Constructs

The synthesis of a series of methylene(methylimino) (MMI) linked oligodeoxyribonucleotide dimers modified at the 2′-position with fluoro and/or methoxy groups and their incorporation into different sequences has been accomplished. From these dimers, bis 2