31356-86-2

Basic information

• Product Name: Uridine, 2'-deoxy-5-iodo-, 3',5'-bis(4-methylbenzoate)
• CAS NO: 31356-86-2
• Molecular Formula: C25H23IN2O7
• Molecular Weight: 590.371
• Mol File: 31356-86-2.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Uridine, 2'-deoxy-5-iodo-, 3',5'-bis(4-methylbenzoate)(CAS DataBase Reference)
• NIST Chemistry Reference: Uridine, 2'-deoxy-5-iodo-, 3',5'-bis(4-methylbenzoate)(31356-86-2)
• EPA Substance Registry System: Uridine, 2'-deoxy-5-iodo-, 3',5'-bis(4-methylbenzoate)(31356-86-2)

Safety Data

• Hazardous Substances Data: 31356-86-2(Hazardous Substances Data)

Upstream product

• 38953-72-9 5-iodo-2,4-bis-O-trimethylsilyluracil 
• 4330-21-6 2-deoxy-3,5-di-O-p-toluoyl-α-D-erythro-pentofuranosyl chloride 
• 54-42-2 5-Iodo-2'-deoxyuridine 
• 874-60-2 4-methyl-benzoyl chloride 
• 951-78-0 2'-deoxyuridine 
• 106-43-4 para-chlorotoluene 
• 4449-38-1 2'-deoxy-3',5'-di-O-(4-methylbenzoyl)uridine 

Downstream Products

• 153865-92-0 5-<3-hydroxy-3-(p-methoxyphenyl)prop-1-ynyl>-3',5'-di-O-(p-toluoyl)-2'-deoxyuridine 
• 77882-22-5 C₃₇H₃₄N₂O₉ 
• 153866-01-4 5-(benzoylethynyl)-3',5'-di-O-(p-toluoyl)-2'-deoxyuridine 
• 77875-88-8 5-Hexynyl-3',5'-di-O-p-toluyl-2'-deoxyuridine 
• 873204-55-8 3',5'-di-O-p-toluoyl-5-(N-tert-butyloxycarbonylindol-2-yl)-2'-deoxyuridine 
• 127235-42-1 β-5-(2''-thienyl)-2'-deoxy-3',5'-di-O-toluoyluridine 
• 85267-64-7 5-(3-Hydroxypropynyl)-3',5'-di-O-p-toluyl-2'-deoxyuridine 
• 153866-00-3 3',5'-di-o-(p-toluoyl)-5-(p-toluoylethynyl)-2'-deoxyuridine 
• 153865-94-2 3',5'-di-O-(p-toluoyl)-5-(o-toluoylethynyl)-2'-deoxyuridine 
• 153865-95-3 5-(p-methoxybenzoylethynyl)-3',5'-di-O-(p-toluoyl)-2'-deoxyuridine 
• 153865-91-9 5-<3-hydroxy-3-(p-tolyl)prop-1-ynyl>-3',5'-di-O-(p-toluoyl)-2'-deoxyuridine 

Relevant articles and documents

Furan decorated nucleoside analogues as fluorescent probes: synthesis, photophysical evaluation, and site-specific incorporation

The synthesis and photophysical evaluation of modified nucleoside analogues in which a five-membered heterocycle (furan, thiophene, oxazole, and thiazole) is attached to the 5-position of 2′-deoxyuridine are reported. The furan-containing derivative is id

5-Propynylamino α-deoxyuridine promotes DNA duplex stabilization of anionic and neutral but not cationic α-oligonucleotides

Incorporation of 5-propynylamino and 5-propynyl α-2′-deoxyuridine into α-oligonucleotides (α-ON) allows high-affinity targeting of complementary DNA for α-ON with anionic and neutral backbone but not for cationic α-ON, revealing clues on the role of the a

Base analogues

Nucleotide or base analogues having structure (3) or (4) wherein X═O or NH or S and each R6is independently H or alkyl or alkenyl or alkoxy or aryl or a reporter moiety.