1294481-79-0

Basic information

• Product Name: (2R)-2-Deoxy-2-fluoro-2-Methyl-D-erythro-pentonic acid-g-lactone 3,5-bis(4-chlorobenzoate)
• Synonyms: (2R)-2-Deoxy-2-fluoro-2-Methyl-D-erythro-pentonic acid-g-lactone 3,5-bis(4-chlorobenzoate);3,5-Di-O-p-chlorobenzoyl-2-deoxy-2-fluoro-2-C-Methyl-D-ribono-γ-lacton;(2R)-2-Deoxy-2-fluoro-2-methyl-D-erythropentonic acid gamama-lactone 3,5-bis(4-chlorobenzoate);((2R,3R,4R)-3-((4-Chlorobenzoyl)oxy)-4-fluoro-4-methyl-5-oxotetrahydrofuran-2-yl)methyl 4-chlorob;[(2R,3R,4R)-3-(4-Chlorobenzoyl)oxy-4-fluoro-4-methyl-5-oxo-tetrahydrofuran-2-yl]methyl 4-chlorobenzoate;d-erythro-pentonic acid, 2-deoxy-2-fluoro-2-methyl-, -lactone, 3,5-bis(4-chlorobenzoate), (2r)-;[(2R,3R,4R)-3-(4-chlorobenzoyl)oxy-4-fluoro-4-methyl-5-oxooxolan-2-yl]methyl 4-chlorobenzoate;3,5-Di-O-p-chlorobenzoyl-2-deoxy-2-fluoro-2-Cmethyl-D-ribono-lactone
• CAS NO: 1294481-79-0
• Molecular Formula: C₂₀H₁₅Cl₂FO₆
• Molecular Weight: 441.2339032
• Product Categories: apis
• Mol File: 1294481-79-0.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 522.7±50.0 °C(Predicted)
• Appearance: /
• Density: 1.47
• Storage Temp.: 2-8°C
• CAS DataBase Reference: (2R)-2-Deoxy-2-fluoro-2-Methyl-D-erythro-pentonic acid-g-lactone 3,5-bis(4-chlorobenzoate)(CAS DataBase Reference)
• NIST Chemistry Reference: (2R)-2-Deoxy-2-fluoro-2-Methyl-D-erythro-pentonic acid-g-lactone 3,5-bis(4-chlorobenzoate)(1294481-79-0)
• EPA Substance Registry System: (2R)-2-Deoxy-2-fluoro-2-Methyl-D-erythro-pentonic acid-g-lactone 3,5-bis(4-chlorobenzoate)(1294481-79-0)

Safety Data

• Hazardous Substances Data: 1294481-79-0(Hazardous Substances Data)

Usage

General Description

(2R)-2-Deoxy-2-fluoro-2-Methyl-D-erythro-pentonic acid-g-lactone 3,5-bis(4-chlorobenzoate) is a synthetic derivative of D-erythro-pentonic acid-g-lactone, which is a precursor to various important bioactive compounds. The compound contains two fluorine atoms and two methyl groups, as well as two 4-chlorobenzoate groups attached to the 3 and 5 positions of the pentonic acid-g-lactone. These chemical features make this compound potentially useful in medicinal chemistry and drug development, as fluorine and methyl groups can improve the metabolic stability and pharmacokinetic properties of drugs, while 4-chlorobenzoate groups can allow for easy detection and purification of the compound. Further research into the biological activity and potential pharmaceutical applications of this compound is warranted.

Upstream product

• 879551-04-9 (3R,4R,5R)-3?fluoro?4?hydroxy?5?(hydroxymethyl)?3?methyltetrahydrofuran?2?one 
• 122-01-0 4-chloro-benzoyl chloride 

Downstream Products

• 1294481-82-5 (2R,3R,4R,5R)-5-(2-amino-6-chloro-9H-purin-9-yl)-2-(((4-chlorobenzoyl)oxy)methyl)-4-fluoro-4-methyltetrahydrofuran-3-yl 4-chlorobenzoate 
• 1294481-81-4 (2R,3R,4R,5R)-5-bromo-2-(((4-chlorobenzoyl)oxy)methyl)-4-fluoro-4-methyltetrahydrofuran-3-yl 4-chlorobenzoate 
• 1294481-80-3 ((2R,3R,4R,5R)-3-((4-chlorobenzoyl)oxy)-4-fluoro-5-hydroxy-4-methyltetrahydrofuran-2-yl)methyl 4-chlorobenzoate 
• 1199809-32-9 PSI-938 
• 1199809-30-7 (2R,3R,4R,5R)-5-(2-amino-6-ethoxy-9H-purin-9-yl)-4-fluoro-2-(hydroxymethyl)-4-methyltetrahydrofuran-3-ol 

Relevant articles and documents

The synthesis of hydroxyaminopurine nucleosied (by machine translation)

A compound or salt thereof having the following structure useful for the treatment of hepatitis C virus (HCV): wherein R 7 is C 1-6 alkyl or C 3-6 cycloalkyl and R 8 is -O(C 1-6 alkyl) or -O(C 3-6 cycloalkyl).