acetofluoro-A-D-glucose - Names and Identifiers
Name | acetofluoro-A-D-glucose
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Synonyms | acetofluoro-A-D-glucose Tetraacetyl-alpha-D-glucose fluoride a-D-Glucopyranosyl fluoride tetraacetate alpha-D-Glucopyranosyl fluoride tetraacetate Tetra-O-acetyl-alpha-D-glucopyranosyl fluoride a-D-Glucopyranosyl fluoride,2,3,4,6-tetraacetate 2,3,4,6-Tetra-O-Acetyl-Alpha-D-Glucopyranosyl Fluoride 2,3,4,6-TETRA-O-ACETYL-ALPHA-D-GLUCOPYRANOSYL FLUORIDE (EP)
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CAS | 3934-29-0
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InChI | InChI=1/C14H19FO9/c1-6(16)20-5-10-11(21-7(2)17)12(22-8(3)18)13(14(15)24-10)23-9(4)19/h10-14H,5H2,1-4H3/t10-,11-,12+,13-,14+/m1/s1 |
acetofluoro-A-D-glucose - Physico-chemical Properties
Molecular Formula | C14H19FO9
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Molar Mass | 350.29 |
Density | 1.30 |
Melting Point | 105.0 to 109.0 °C |
Boling Point | 374.8±42.0 °C(Predicted) |
Flash Point | 174.346°C |
Solubility | soluble in Chloroform |
Vapor Presure | 0mmHg at 25°C |
Appearance | powder to crystal |
Color | White to Almost white |
Storage Condition | Sealed in dry,2-8°C |
Refractive Index | 1.465 |
MDL | MFCD00792705 |
acetofluoro-A-D-glucose - Risk and Safety
WGK Germany | 3 |
HS Code | 29329990 |
acetofluoro-A-D-glucose - Introduction
acetofluoro-A-D-glucose (acetofluoro-α-D-glucose) is an organic compound whose chemical formula is C10H14O6F.
Nature:
-Appearance: Colorless solid
-Solubility: Soluble in organic solvents, such as methanol, dimethyl sulfoxide, slightly soluble in water
-melting point: about 160-165 ℃
-relative molecular mass: 270.22g/mol
Use:
-Chemical research: It can be used as an intermediate in organic synthesis and used in the synthesis of organic compounds, such as drugs, pesticides, dyes, etc.
-Medical field: It may have anti-diabetic, anti-viral and anti-tumor activities, so it also has potential application value in medical research.
Preparation Method:
There are many ways to prepare this compound. Common methods include:
1. The glucopyranose is reacted with an acetylating agent (such as acetic anhydride) under acidic conditions to generate 2,3,4,6-tetra-O-acetyl-α-D-glucopyranose.
2. Next, the obtained acetylated product is reacted with a fluorinating agent such as stannous fluoride to replace the oxygen atom (O) at the position of the hydroxyl group (OH) therein with a fluorine atom (F), thereby obtaining a acetofluoro-A-D-glucose.
Safety Information:
-The toxicity and irritation data of this compound are limited, so it is necessary to follow general laboratory safety practices.
-If the compound needs to be added to a product or drug, corresponding safety evaluation and testing are required to ensure the safety of use.
Please note that this compound is only used for research and experimental purposes and should be used in accordance with relevant laws and regulations and in a safe environment.
Last Update:2024-04-09 20:49:11