5-iodo-2′-deoxyuridine

Structural formula

Business number	016D
Molecular formula	C9H11IN2O5
Molecular weight	354.1
label	2-deoxy-5′-iodouridine, 5′-iodo-2-deoxyuridine, 5′-iododeoxyuracil nucleoside, Herpes net; iodine deoxyuridine, 1-(2-Deoxy-β-D-ribofuranosyl)-5-iodouracil, 2′-Deoxy-5-iodouridine, antiviral drugs

• Numbering system
• Physical property data
• Toxicological data
• Ecological data
• Molecular structure data
• Computing chemical data
• More
  • Properties and Stability
  • Storage method
  • Synthesis method
  • Purpose

Numbering system

CAS number:54-42-2

MDL number:MFCD00134656

EINECS number:200-207-8

RTECS number:YU7700000

BRN number:30397

PubChem number:24896108

Physical property data

1. Properties: White crystalline powder.

2. Density (g/mL, 25/4℃): Undetermined

3. Relative vapor density (g/mL, air=1): Undetermined

4. Melting point (ºC): 176~184℃ (decomposition)

5. Boiling point (ºC, normal pressure): Undetermined

6. Boiling point (ºC, normal pressure) 5.2kPa): Not determined

7. Refractive index: Not determined

8. Flash point (ºC): Not determined

9. Specific rotation ( º): [α]_D²⁵+7.4° (C=0.108, in water), [α]_D^{20 sup>+29.0° (C=1, in 1mol/L sodium carbonate)}

10. Autoignition point or ignition temperature (ºC): Undetermined

11. Vapor pressure ( kPa, 25ºC): Undetermined

12. Saturated vapor pressure (kPa, 60ºC): Undetermined

13. Heat of combustion (KJ/mol): Undetermined

14. Critical temperature (ºC): Undetermined

15. Critical pressure (KPa): Undetermined

16. Oil-water (octanol/water) partition coefficient relationship Value: Undetermined

17. Explosion upper limit (%, V/V): Undetermined

18. Explosion lower limit (%, V/V): Undetermined

19. Solubility: Solubility at 25°C (mg/ml): water 2, ethanol 2.6, ether 0.014, chloroform 0.03, acetone 1.6, ethyl acetate 1.8, dioxane 5.7. It is easily soluble in dilute sodium hydroxide solution and slightly soluble in dilute hydrochloric acid. The aqueous solution is more stable when it is acidic than when it is alkaline.

Toxicological data

None

Ecological data

None

Molecular structure data

5. Molecular property data:

1. Molar refractive index: 64.75

2. Molar volume (cm³/mol): 164.8

3. Isotonic specific volume (90.2K): 504.2

4. Surface tension (dyne/cm): 87.4

5. Polarizability (10^{– 24}cm³): 25.66

Compute chemical data

1. Hydrophobic parameter calculation reference value (XlogP): -1

2. Number of hydrogen bond donors: 3

3. Number of hydrogen bond acceptors: 5

4. Number of rotatable chemical bonds: 2

5. Number of tautomers: 3

6. Topological molecular polar surface area (TPSA): 99.1

7. Number of heavy atoms: 17

8. Surface charge: 0

9. Complexity: 386

10. Isotopic atoms Quantity: 0

11. Determine the number of atomic stereocenters: 3

12. Uncertain number of atomic stereocenters: 0

13. Determine chemical bond positions Number of stereocenters: 0

14. Number of uncertain chemical bond stereocenters: 0

15. Number of covalent bond units: 1

Properties and stability

None

Storage method

This product should be sealed and stored in a dry place at 4°C away from light.

Synthesis method

1. There are many production methods. Starting from propargyl alcohol, through oxidation; esterification, and then cyclization with 2- aminooxazoline nucleoside, can be obtained 2,2-oxo-pyrimidine nucleoside is then acylated, brominated, catalytically hydrogenated, and hydrolyzed to obtain iodine glycoside. 5′- deoxycytosine nucleotides can be prepared from fish essence, and iodine glycosides can also be prepared after further processing.

2.

Purpose

1. Used for biochemical research. Tracheitis virus testing. Treat herpes simplex keratitis.

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