CAS 1582-79-2

Formula: C23H17Cl2FN2O7

InChI: InChI=1S/C23H17Cl2FN2O7/c24-14-5-1-12(2-6-14)21(30)33-11-18-17(35-22(31)13-3-7-15(25)8-4-13)9-19(34-18)28-10-16(26)20(29)27-23(28)32/h1-8,10,17-19H,9,11H2,(H,27,29,32)/t17-,18+,19+/m0/s1

InChI key: OGKGUIKIBDTIHT-IPMKNSEASA-N

SMILES: C1[C@@H]([C@H](O[C@H]1N2C=C(C(=O)NC2=O)F)COC(=O)C3=CC=C(C=C3)Cl)OC(=O)C4=CC=C(C=C4)Cl

3,5-Di-O-p-chlorobenzoyl Alpha,Beta-Floxuridine-13C,15N2

Controlled Product

CAS: 110558-30-0, 1582-79-2

Formula: C₂₂CH₁₇Cl₂FN₂O₇

Color and Shape: Neat

Molecular weight: 526.27

Ref: TR-D432277

3,5-Di-O-p-chlorobenzoyl Floxuridine-13C,15N2

Controlled Product

CAS: 1582-79-2

Formula: CC₂₂H₁₇Cl₂F₁₅N₂O₇

Color and Shape: Neat

Molecular weight: 526.274

Ref: TR-D432282

3,5-Di-O-p-chlorobenzoyl Floxuridine

Controlled Product

CAS: 1582-79-2

Formula: C₂₃H₁₇Cl₂FN₂O₇

Color and Shape: Neat

Molecular weight: 523.29

Ref: TR-D432280

3',5'-Di-O-p-chlorobenzoyl-2'-deoxy-5-fluorouridine

CAS: 1582-79-2

3',5'-Di-O-p-chlorobenzoyl-2'-deoxy-5-fluorouridine is a nucleoside derivative that has antiviral activity. It is synthesized by the condensation of 2,3,5-trihydroxybenzoic acid with 3'-chloro-5'-fluoroacetophenone in the presence of pyridine and triethylamine. The nucleoside has been shown to be an effective inhibitor of HIV replication in vitro. 3',5'-Di-O-p-chlorobenzoyl-2'-deoxy-5-fluorouridine also inhibits DNA synthesis in human lymphocytes at concentrations of 5 μM or less. This compound can be used as an activator for DNA polymerases and phosphoramidites for DNA synthesis.

Formula: C₂₃H₁₇Cl₂FN₂O₇

Purity: Min. 95%

Molecular weight: 523.29 g/mol

Ref: 3D-ND22463