(R)-2-Amino-1,1,3-triphenyl-1-propanol
≥98%,≥99% e.e.
- Product Code: 71010
CAS:
86906-05-0
| Molecular Weight: | 303.4 g./mol | Molecular Formula: | C₂₁H₂₁NO |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 142-144°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in the field of asymmetric synthesis, where it serves as a chiral auxiliary or ligand in catalytic reactions. Its unique structure, featuring three phenyl groups and a hydroxyl group, makes it effective in inducing chirality in organic transformations, particularly in the synthesis of enantiomerically pure compounds. It is often employed in the preparation of pharmaceuticals, where the control of stereochemistry is crucial for the efficacy and safety of the drug. Additionally, it finds use in the development of chiral catalysts for various organic reactions, including hydrogenation and carbon-carbon bond formation. Its role in these processes highlights its importance in producing high-value chemicals with specific stereochemical requirements.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | WHITE SOLID |
| PURITY | 98 |
| CHLOROFORM | 82-88 |
| MELTING POINT | 140-145 |
| PURITY ee | 99 |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | Ft23,487.56 |
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| 0.500 | 10-20 days | Ft81,667.74 |
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| 1.000 | 10-20 days | Ft138,770.51 |
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(R)-2-Amino-1,1,3-triphenyl-1-propanol
This compound is primarily utilized in the field of asymmetric synthesis, where it serves as a chiral auxiliary or ligand in catalytic reactions. Its unique structure, featuring three phenyl groups and a hydroxyl group, makes it effective in inducing chirality in organic transformations, particularly in the synthesis of enantiomerically pure compounds. It is often employed in the preparation of pharmaceuticals, where the control of stereochemistry is crucial for the efficacy and safety of the drug. Additionally, it finds use in the development of chiral catalysts for various organic reactions, including hydrogenation and carbon-carbon bond formation. Its role in these processes highlights its importance in producing high-value chemicals with specific stereochemical requirements.
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