(S)-3-(tert-Butyl)-4-(2,6-dimethoxy-3,5-dimethylphenyl)-2,3-dihydrobenzo[d][1,3]oxaphosphole
97%,≥99% ee
- Product Code: 96571
CAS:
2021202-03-7
| Molecular Weight: | 358.41 g./mol | Molecular Formula: | C₂₁H₂₇O₃P |
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| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, particularly as a chiral ligand or catalyst in asymmetric reactions. Its unique structure, featuring a dihydrobenzo[d][1,3]oxaphosphole core, makes it effective in facilitating enantioselective transformations, which are crucial for producing optically active compounds. These compounds are often intermediates in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Additionally, its sterically hindered tert-butyl group and methoxy-substituted aromatic ring enhance its stability and selectivity in catalytic processes, making it a valuable tool for chemists aiming to achieve high enantiomeric purity in their products.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.025 | 10-20 days | $180.36 |
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| 0.100 | 10-20 days | $442.54 |
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| 0.500 | 10-20 days | $1,807.68 |
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(S)-3-(tert-Butyl)-4-(2,6-dimethoxy-3,5-dimethylphenyl)-2,3-dihydrobenzo[d][1,3]oxaphosphole
This chemical is primarily utilized in the field of organic synthesis, particularly as a chiral ligand or catalyst in asymmetric reactions. Its unique structure, featuring a dihydrobenzo[d][1,3]oxaphosphole core, makes it effective in facilitating enantioselective transformations, which are crucial for producing optically active compounds. These compounds are often intermediates in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Additionally, its sterically hindered tert-butyl group and methoxy-substituted aromatic ring enhance its stability and selectivity in catalytic processes, making it a valuable tool for chemists aiming to achieve high enantiomeric purity in their products.
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