(-)-4,5-Bis[hydroxy(diphenyl)methyl]-2,2-dimethyl-1,3-dioxolane
97.0%
- Product Code: 70778
Alias:
(-)-2,3-O-Isopropylidene-1,1,4,4-tetraphenyl-L-threitol
(4R,5R)-4,5-bis(diphenylhydroxymethyl)-2,2-dimethyldioxolane
1,1,4,4-Tetraphenyl-2,3-O-isopropylidene-L-threitol
TADDOL
CAS:
93379-48-7
| Molecular Weight: | 466.58 g./mol | Molecular Formula: | C₃₁H₃₀O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00064467 | |
| Melting Point: | 193-195 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of asymmetric synthesis, where it serves as a chiral auxiliary or ligand. Its structure, featuring two hydroxy(diphenyl)methyl groups, makes it effective in inducing chirality in chemical reactions, particularly in the formation of enantiomerically pure products. It is often employed in catalytic processes, such as asymmetric hydrogenation and carbon-carbon bond-forming reactions, where high enantioselectivity is crucial. Additionally, its stability and steric properties make it suitable for use in organometallic chemistry, aiding in the development of novel catalysts for pharmaceutical and fine chemical synthesis.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | WHITE SOLID |
| PURITY | 97 |
| SPECIFIC ROTATION A20DC1 CHCL3 | -71--62 |
| MELTING POINT | 194-198 |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿570.00 |
+
-
|
| 5.000 | 10-20 days | ฿2,100.00 |
+
-
|
| 25.000 | 10-20 days | ฿9,080.00 |
+
-
|
(-)-4,5-Bis[hydroxy(diphenyl)methyl]-2,2-dimethyl-1,3-dioxolane
This compound is primarily utilized in the field of asymmetric synthesis, where it serves as a chiral auxiliary or ligand. Its structure, featuring two hydroxy(diphenyl)methyl groups, makes it effective in inducing chirality in chemical reactions, particularly in the formation of enantiomerically pure products. It is often employed in catalytic processes, such as asymmetric hydrogenation and carbon-carbon bond-forming reactions, where high enantioselectivity is crucial. Additionally, its stability and steric properties make it suitable for use in organometallic chemistry, aiding in the development of novel catalysts for pharmaceutical and fine chemical synthesis.
| 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 :