(S)-3-(tert-Butyl)-4-(2,6-dimethoxyphenyl)-2,2-dimethyl-2,3-dihydrobenzo[d][1,3]oxaphosphole
97%,≥99% ee
- Product Code: 96554
CAS:
2227217-19-6
| Molecular Weight: | 358.41 g./mol | Molecular Formula: | C₂₁H₂₇O₃P |
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| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in the field of organic synthesis, particularly as a chiral ligand or catalyst in asymmetric reactions. Its unique structure, featuring a phosphole ring and stereocenter, makes it highly effective in facilitating enantioselective transformations, such as hydrogenation or carbon-carbon bond-forming reactions. This enables the production of chiral molecules with high enantiomeric purity, which is crucial in the pharmaceutical industry for developing active pharmaceutical ingredients (APIs) with specific stereochemistry. Additionally, its stability and selectivity make it a valuable tool in academic research for exploring new synthetic methodologies and understanding reaction mechanisms.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.025 | 10-20 days | $150.53 |
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| 0.100 | 10-20 days | $451.58 |
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| 0.500 | 10-20 days | $2,078.90 |
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(S)-3-(tert-Butyl)-4-(2,6-dimethoxyphenyl)-2,2-dimethyl-2,3-dihydrobenzo[d][1,3]oxaphosphole
This compound is primarily utilized in the field of organic synthesis, particularly as a chiral ligand or catalyst in asymmetric reactions. Its unique structure, featuring a phosphole ring and stereocenter, makes it highly effective in facilitating enantioselective transformations, such as hydrogenation or carbon-carbon bond-forming reactions. This enables the production of chiral molecules with high enantiomeric purity, which is crucial in the pharmaceutical industry for developing active pharmaceutical ingredients (APIs) with specific stereochemistry. Additionally, its stability and selectivity make it a valuable tool in academic research for exploring new synthetic methodologies and understanding reaction mechanisms.
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