601512-77-0

Basic information

• Product Name: C₂₄H₂₁FN₂O₇
• CAS NO: 601512-77-0
• Molecular Weight: 468.438
• Mol File: 601512-77-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: C₂₄H₂₁FN₂O₇(CAS DataBase Reference)
• NIST Chemistry Reference: C₂₄H₂₁FN₂O₇(601512-77-0)
• EPA Substance Registry System: C₂₄H₂₁FN₂O₇(601512-77-0)

Safety Data

• Hazardous Substances Data: 601512-77-0(Hazardous Substances Data)

Upstream product

• 28279-75-6 methyl 2-deoxy-3,5-di-O-benzoyl-2-fluoro-β-D-xylofuranoside 
• 65-71-4 thymin 
• 601512-75-8 1-O-acetyl-2-deoxy-2-fluoro-3,5-di-O-benzoyl-α,β-D-xylofuranose 
• 7288-28-0 2,4-bis(trimethylsiloxy)-5-methylpyrimidine 

Downstream Products

• 601512-80-5 1-[2-deoxy-5-O-(4,4'-dimethoxytrityl)-2-fluoro-β-D-xylofuranosyl]thymine 
• 601512-79-2 1-(2-deoxy-2-fluoro-β-D-xylofuranosyl)thymine 

Relevant articles and documents

XNA ?(xylo nucleic acid): A summary and new derivatives

Fully modified homopyrimidine 2′-deoxy-xylo nucleic acid (dXNA) form triple helixes with complementary DNA/RNA with thermal stabilities comparable to those of the corresponding DNA:DNA and DNA:RNA duplexes. However, a single or few insertions of dXNA monomers in a DNA strand significantly lower duplex stabilities. The dXNA monomers are known to adopt predominantly an N-type furanose conformation in solution. With a desire to increase the binding affinity, seven sugar-modified XNA monomers (H, F, N, M, K, P and Q) have been synthesised and their effect on hybridization towards DNA and RNA complements studied. The introduction of 2′-fluoro and 2′-hydroxy substituents was expected to induce conformational restriction towards C3′-endo-type furanose conformation of monomer F derived from 1-(2′-deoxy-2′-fluoro-β-D-xylofuranosyl)thymine and monomer H derived from 1-(β-D-xylofuranosyl)thymine. The presence of functionalites facing the minor groove as in 1-(2′-amino-2′-deoxy-2′-N, 4′-C-methylene-β-D-xylofuranosyl)thymine (monomer N), 1-[4-C-(N-methylpiperazinyl)methyl-β-D-xylofuranosyl]thymine (monomer P), 1-(4-C-piperazinylmethyl-β-D-xylofuranosyl)thymine (monomer Q), 1-(4-C-hydroxymethyl-β-D-xylofuranosyl)thymine (monomer M) and 9-(4-C-hydroxymethyl-β-D-xylofuranosyl)adenine (monomer K) was studied, with monomer N being locked in an N-type furanose conformation. Besides, an efficient synthesis of known xylo-LNA phosphoramidite 19, required for the incorporation of 1-(2′-O,4′-C-methylene-β-D-xylofuranosyl)thymine (monomer L) is described. For comparison, hydridization data of various XNAs reported in the literature are included in the discussion section. The thermal denaturation studies show that XNAs containing conformationally locked monomers (N and L) display improved binding affinity, and that partially modified DNA/XNA chimera, or fully modified XNA display preferential hybridization towards RNA complements. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2005.

Xylo-configured oligonucleotides (XNA, xylo nucleic acid): Synthesis of conformationally restricted derivatives and hybridization towards DNA and RNA complements

Xylo-Configured oligonucleotides (XNA) containing a novel conformationally restricted 2′-deoxy-2′-fluoro-β-D-xylofuranosyl nucleotide monomer, a novel conformationally locked 2′-amino-2′-deoxy-2′-N,4′-C-methylene-β-D- xylofuranosyl nucleotide monomer, and