Welcome to LookChem.com Sign In|Join Free

CAS

  • or
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. This complex chemical compound features a deoxyribose sugar derivative with difluoro and dibenzoate substitutions, along with a methanesulfonate group. The presence of these functional groups can alter the chemical and biological properties of the compound, making it a candidate for research and pharmaceutical applications.

12211-11-9 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 2-Deoxy-2,2-difluoro-D-ribofuranose-3,5-dibenzoate-1-methanesulfonate Manufacturer/High quality/Best price/In stock

    Cas No: 12211-11-9

  • USD $ 3.0-3.0 / Kilogram

  • 1 Kilogram

  • 1-100 Metric Ton/Month

  • Dayang Chem (Hangzhou) Co.,Ltd.
  • Contact Supplier
  • 12211-11-9 Structure
  • Basic information

    1. Product Name: 2-DEOXY-2,2-DIFLUORO-D-RIBOFURANOSE-3,5-DIBENZOATE-1-METHANESULFONATE
    2. 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)
    3. CAS NO:12211-11-9
    4. Molecular Formula: C20H18F2O8S
    5. Molecular Weight: 456.416
    6. EINECS: N/A
    7. Product Categories: INTERMEDIATESOFGEMCITABINE
    8. Mol File: 12211-11-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 588.439 °C at 760 mmHg
    3. Flash Point: 309.677 °C
    4. Appearance: /
    5. Density: 1.464 g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-DEOXY-2,2-DIFLUORO-D-RIBOFURANOSE-3,5-DIBENZOATE-1-METHANESULFONATE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-DEOXY-2,2-DIFLUORO-D-RIBOFURANOSE-3,5-DIBENZOATE-1-METHANESULFONATE(12211-11-9)
    11. EPA Substance Registry System: 2-DEOXY-2,2-DIFLUORO-D-RIBOFURANOSE-3,5-DIBENZOATE-1-METHANESULFONATE(12211-11-9)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 12211-11-9(Hazardous Substances Data)

12211-11-9 Usage

Uses

Used in Pharmaceutical Research:
2-Deoxy-2,2-difluoro-D-ribofuranose-3,5-dibenzoate-1-methanesulfonate is used as a research compound for exploring its potential in pharmaceutical applications. The difluoro and dibenzoate substitutions may confer unique properties to the molecule, which could be harnessed for the development of new drugs or drug candidates.
Used in Biochemical Studies:
In the field of biochemistry, 2-Deoxy-2,2-difluoro-D-ribofuranose-3,5-dibenzoate-1-methanesulfonate is used as a tool to study the interactions of ribose derivatives with biological systems. The modifications to the ribose sugar may provide insights into the role of sugar components in various biochemical processes and their potential as therapeutic agents.
Used in Drug Development:
2-Deoxy-2,2-difluoro-D-ribofuranose-3,5-dibenzoate-1-methanesulfonate is utilized in drug development as a lead compound or a structural component in the design of new pharmaceuticals. The synthetic nature of the compound allows for further modifications and optimization to enhance its pharmacological properties and therapeutic potential.
Used in Chemical Synthesis:
In the chemical synthesis industry, 2-Deoxy-2,2-difluoro-D-ribofuranose-3,5-dibenzoate-1-methanesulfonate serves as a starting material or an intermediate in the synthesis of more complex molecules. Its unique structure and functional groups can be used to create a variety of chemical entities with diverse applications.
Used in Analytical Chemistry:
2-Deoxy-2,2-difluoro-D-ribofuranose-3,5-dibenzoate-1-methanesulfonate is employed in analytical chemistry as a reference compound or a standard for the development and validation of analytical methods. Its distinct chemical properties can be used to evaluate the performance of chromatographic, spectroscopic, or other analytical techniques.

Check Digit Verification of cas no

The CAS Registry Mumber 12211-11-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,2,2,1 and 1 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 12211-11:
(7*1)+(6*2)+(5*2)+(4*1)+(3*1)+(2*1)+(1*1)=39
39 % 10 = 9
So 12211-11-9 is a valid CAS Registry Number.

12211-11-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-DEOXY-2,2-DIFLUORO-D-RIBOFURANOSE-3,5-DIBENZOATE

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:12211-11-9 SDS

12211-11-9Upstream product

12211-11-9Downstream Products

12211-11-9Relevant articles and documents

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

Cai, Yanqing,Liu, Hongxia,Xu, Qian,Song, Qiushi,Liu, Huijun

, p. 31648 - 31655 (2015)

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.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 12211-11-9