(DHQD)2PHAL
95%
- Product Code: 62469
CAS:
140853-10-7
| Molecular Weight: | 778.98 g./mol | Molecular Formula: | C₄₈H₅₄N₆O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00198107 | |
| Melting Point: | 160 °C (dec.)(lit.) | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is widely used as a chiral ligand in asymmetric synthesis, particularly in catalytic enantioselective reactions. It is highly effective in facilitating the Sharpless asymmetric dihydroxylation of alkenes, which is a key step in the production of chiral diols. These diols are important intermediates in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. The ligand's ability to induce high enantioselectivity makes it valuable in creating optically active compounds, which are crucial for the development of drugs with specific biological activities. Its application extends to organic chemistry research, where it aids in the exploration of new synthetic pathways and the optimization of existing processes for producing chiral molecules.
Product Specification:
| Test | Specification |
|---|---|
| Purity (GC) | 95-100 |
| Methanol | -265 to -260 |
| Melting point | 158-162 |
| Appearance | Off-white to yellow solid |
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 5g | 10-20 days | ฿11,590.00 |
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| 200mg | 10-20 days | ฿720.00 |
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| 1g | 10-20 days | ฿2,890.00 |
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(DHQD)2PHAL
This chemical is widely used as a chiral ligand in asymmetric synthesis, particularly in catalytic enantioselective reactions. It is highly effective in facilitating the Sharpless asymmetric dihydroxylation of alkenes, which is a key step in the production of chiral diols. These diols are important intermediates in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. The ligand's ability to induce high enantioselectivity makes it valuable in creating optically active compounds, which are crucial for the development of drugs with specific biological activities. Its application extends to organic chemistry research, where it aids in the exploration of new synthetic pathways and the optimization of existing processes for producing chiral molecules.
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