(2R,3R,4R)-2,3,5-Tris(benzyloxy)-4-hydroxypentanal
95%
- Product Code: 103600
CAS:
54623-25-5
| Molecular Weight: | 420.50 g./mol | Molecular Formula: | C₂₆H₂₈O₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03425640 | |
| Melting Point: | Boiling Point: | 591.5°C at 760 mmHg | |
| Density: | Storage Condition: | -20℃, inert gas storage |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in the preparation of complex carbohydrates and glycoconjugates. Its structure, featuring multiple benzyl-protected hydroxyl groups, makes it a valuable intermediate in the synthesis of oligosaccharides and other biologically active molecules. It is often employed in the construction of glycosidic linkages, where its hydroxyl groups can be selectively deprotected and functionalized. Additionally, it serves as a chiral building block in the synthesis of natural products and pharmaceuticals, enabling the creation of stereochemically defined structures. Its application extends to research in glycobiology, where it aids in studying carbohydrate-protein interactions and developing glycan-based therapeutics.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White Powder |
| Purity (%) | 94.5-100 |
| Melting Point | 48.0-55.0 |
| Optical Rotation (C=4 In DCM) | 59.0 Degree Celsius-67.0 Degree Celsius |
| Infrared Spectrum | Conforms To Structure |
| NMR | Conforms To Structure |
| Note | This Product Is Low Melting Point Solid, May Change State In Different Environments (Solid, Liquid Or Semi-Solid) |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $14.92 |
+
-
|
| 0.250 | 10-20 days | $18.08 |
+
-
|
| 1.000 | 10-20 days | $48.37 |
+
-
|
(2R,3R,4R)-2,3,5-Tris(benzyloxy)-4-hydroxypentanal
This compound is primarily utilized in organic synthesis, particularly in the preparation of complex carbohydrates and glycoconjugates. Its structure, featuring multiple benzyl-protected hydroxyl groups, makes it a valuable intermediate in the synthesis of oligosaccharides and other biologically active molecules. It is often employed in the construction of glycosidic linkages, where its hydroxyl groups can be selectively deprotected and functionalized. Additionally, it serves as a chiral building block in the synthesis of natural products and pharmaceuticals, enabling the creation of stereochemically defined structures. Its application extends to research in glycobiology, where it aids in studying carbohydrate-protein interactions and developing glycan-based therapeutics.
| Mechanism | - |
| Appearance | - |
| Longevity | - |
| Strength | - |
| Storage | - |
| Shelf Life | - |
| Allergen(s) | - |
| Dosage (Range) | - |
| Recommended Dosage | - |
| Dosage (Per Day) | - |
| Recommended Dosage (Per Day) | - |
| Mix Method | - |
| Heat Resistance | - |
| Stable in pH range | - |
| Solubility | - |
| Product Types | - |
| INCI | - |
Cart
No products
Subtotal:
$0.00
$0.00
Total :