Inert atmosphere, store in freezer, under -20ºC.
(-)-2,3-O-Isopropylidene-D-Threitol -2,3-O-Isopropylidene-D-Threitol.png)
Catalog Number OM-5435
Product Name (-)-2,3-O-Isopropylidene-D-Threitol
CAS No. 73346-74-4
Size 1 g; 5 g;
Aspect White solid
| CAS No. | 73346-74-4 |
| Molecular Formula | C7H14O4 |
| MW | 162.18 |
| Melting Point | 48-51ºC(lit.) |
| Boiling Point | 91-93ºC(lit.) |
| Application | Pharmaceutical intermediates. |
| Stability | Stable. Incompatible with strong oxidizing agents. |
| Solubility | Soluble in water. |
| Synonyms | (-)-2,3-O-isopropylidene-D-threitol, (4R,5R)-4,5-bis(hydroxymethyl)-2,2-dimethyl-1,3-dioxolane, (4R,5R)-(-)-2,2-dimethyl-1,3-dioxolane-4,5-dimethanol, 2,3-O-isopropylidene-D-threitol |
| MDL | MFCD00009761 |
| Safety Description | S22;S24/25;S36; |
| R-phrases | R20/21/22;R36/37/38; |
| SMILES | CC1(OC(C(O1)CO)CO)C |
| InchiKey | INVRLGIKFANLFP-UHFFFAOYSA-N |
Inert atmosphere, store in freezer, under -20ºC.
·High Purity: Our 2-Deoxy-2-(1-oxo-4-pentyn-1-ylamino)-D-glucopyranose is synthesized with exceptional purity, ensuring minimal contaminants for accurate and reproducible experimental results.
·Unique Structure: The presence of a pentynylamino group at the 2-deoxy position provides a distinctive chemical handle for further functionalization and conjugation reactions.
·Stable under Storage: Exhibits good stability when stored under recommended conditions, preserving its reactivity over time.
·Bioconjugation: Ideal for attaching to proteins, peptides, or other biomolecules via click chemistry for use in drug delivery, imaging, or diagnostic applications.
·Glycoscience Research: Used to study carbohydrate-protein interactions, glycosylation pathways, and enzyme specificities.
·Material Science: Incorporated into polymers or hydrogels for the development of novel biomaterials with specific functionalities.
·2,3-O-Isopropylidene-D-Glycerol: A similar compound used in the synthesis of glycerol derivatives and other bioactive molecules.
·2,3-O-Isopropylidene-L-Threitol: The L-enantiomer of this compound, used in the synthesis of chiral compounds and pharmaceutical intermediates.
·1,4-Di-O-tosyl-2,3-O-isopropylidene-D-threitol: A derivative with tosyl groups, used in more complex chemical syntheses.
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