It often serves as a carbohydrate intermediate in organic synthesis, enabling selective functionalization for the preparation of complex sugars or glycosylated pharmaceuticals. The triacetate protection allows reactions at other positions while preventing undesired side reactions. 2,6-Anhydro-5-deoxy-D-arabino-hex-5-enitol triacetate is a protected sugar derivative in which the hydroxyl groups are acetylated and a 2,6-anhydro ring structure is present.
2,6-anhydro-5-deoxy-D-arabino-hex-5-enitol triacetate
| API Name | Acyclovir |
|---|---|
| CAS No | 4098-06-0 |
| Molecular Formula | C12H16O7 |
| Molecular Weight | 272.25 g/mol |
| Synonyms | [(2R,3R,4R)-3,4-diacetyloxy-3,4-dihydro-2H-pyran-2-yl]methyl acetate |
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Frequently Asked Questions
It often serves as a carbohydrate intermediate in organic synthesis, enabling selective functionalization for the preparation of complex sugars or glycosylated pharmaceuticals. The triacetate protection allows reactions at other positions while preventing undesired side reactions. 2,6-Anhydro-5-deoxy-D-arabino-hex-5-enitol triacetate is a protected sugar derivative in which the hydroxyl groups are acetylated and a 2,6-anhydro ring structure is present.
The CAS number of 2,6-anhydro-5-deoxy-D-arabino-hex-5-enitol triacetate is 4098-06-0.
The molecular formula of 2,6-anhydro-5-deoxy-D-arabino-hex-5-enitol triacetate is C12H16O7.
The listed molecular weight of 2,6-anhydro-5-deoxy-D-arabino-hex-5-enitol triacetate is 272.25 g/mol.
2,6-anhydro-5-deoxy-D-arabino-hex-5-enitol triacetate is listed as being used in connection with the following API: Acyclovir.
The listed synonym or IUPAC name for 2,6-anhydro-5-deoxy-D-arabino-hex-5-enitol triacetate is [(2R,3R,4R)-3,4-diacetyloxy-3,4-dihydro-2H-pyran-2-yl]methyl acetate.