12211-11-9

Basic information

• Product Name: 2-DEOXY-2,2-DIFLUORO-D-RIBOFURANOSE-3,5-DIBENZOATE-1-METHANESULFONATE
• Synonyms: 2-Deoxy-2,2-difluoro-3,5-dibenzoyl-D-ribofuranose-1-methanesulfonate;2-deoxy-2,2-difluoro-D-erythro-pentofuranos-1-ulose-3,5-dibenzoate-1-methanesulfonate (T8)
• CAS NO: 12211-11-9
• Molecular Formula: C20H18F2O8S
• Molecular Weight: 456.416
• Product Categories: INTERMEDIATESOFGEMCITABINE
• Mol File: 12211-11-9.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 588.439 °C at 760 mmHg
• Flash Point: 309.677 °C
• Appearance: /
• Density: 1.464 g/cm³
• CAS DataBase Reference: 2-DEOXY-2,2-DIFLUORO-D-RIBOFURANOSE-3,5-DIBENZOATE-1-METHANESULFONATE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-DEOXY-2,2-DIFLUORO-D-RIBOFURANOSE-3,5-DIBENZOATE-1-METHANESULFONATE(12211-11-9)
• EPA Substance Registry System: 2-DEOXY-2,2-DIFLUORO-D-RIBOFURANOSE-3,5-DIBENZOATE-1-METHANESULFONATE(12211-11-9)

Safety Data

• Hazardous Substances Data: 12211-11-9(Hazardous Substances Data)

Usage

General Description

2-Deoxy-2,2-difluoro-D-ribofuranose-3,5-dibenzoate-1-methanesulfonate is a complex chemical compound containing a deoxyribose sugar derivative with difluoro and dibenzoate substitutions. It also includes a methanesulfonate group. 2-Deoxy-2,2-difluoro-D-ribofuranose-3,5-dibenzoate-1-methanesulfonate is a synthetic derivative of ribofuranose, a sugar component found in RNA and other bioactive molecules, with various substitutions and modifications. The presence of difluoro and dibenzoate groups can impact the chemical and biological properties of this compound, making it potentially useful for research and pharmaceutical applications.

Upstream product

• 7440-67-7 zirconium 

Relevant articles and documents

Investigation of the reaction progress between stannous chloride and zirconium in molten LiCl-KCl

LiCl-KCl-ZrCl4 melt was prepared by an in situ displacement reaction between SnCl2 and Zr in LiCl-KCl melt at 773 K, and the progress of the reaction between SnCl2 and Zr was also investigated by dynamic electrochemical measurements, such as cyclic voltammetry, square wave voltammetry and open circuit chronopotentiometry. The results reveal that the concentration of Zr(iv) increases gradually and reaches a maximum value with the reaction time increasing from 0 to 210 min, while the concentration of Sn(ii) decreases gradually and drops below the detection limit. In addition, the chemical analyses of Zr(iv) and Sn(ii) in the melt at various times were also carried out and the results are in good agreement with those of the electrochemical measurements. Finally, LiCl-KCl-ZrCl4 melts with a low concentration of Sn(ii) (0.01 wt%) were obtained, when the reaction time was prolonged to 210 min.