(11bR)-2,6-Bis(3,5-dichlorophenyl)-4-hydroxy-4-oxide-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin
98%
- Product Code: 70127
CAS:
1191451-24-7
| Molecular Weight: | 638.3 g./mol | Molecular Formula: | C₃₂H₁₇Cl₄O₄P |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 825.7±75.0 °C | |
| Density: | 1.62±0.1 g/mL | Storage Condition: | room temperature, dry |
Product Description:
Primarily utilized in the field of organic synthesis, this compound serves as a key intermediate in the production of complex organic molecules. Its unique structure allows it to act as a catalyst or a reagent in various chemical reactions, particularly in the formation of carbon-phosphorus bonds. This makes it valuable in the development of pharmaceuticals, where such bonds are often crucial for the biological activity of drugs. Additionally, it is employed in the synthesis of advanced materials, including polymers and coatings, where its properties can enhance durability and performance. The compound's ability to participate in stereospecific reactions also makes it useful in the creation of chiral molecules, which are important in the production of enantiomerically pure substances for medical and industrial applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $187.52 |
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(11bR)-2,6-Bis(3,5-dichlorophenyl)-4-hydroxy-4-oxide-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin
Primarily utilized in the field of organic synthesis, this compound serves as a key intermediate in the production of complex organic molecules. Its unique structure allows it to act as a catalyst or a reagent in various chemical reactions, particularly in the formation of carbon-phosphorus bonds. This makes it valuable in the development of pharmaceuticals, where such bonds are often crucial for the biological activity of drugs. Additionally, it is employed in the synthesis of advanced materials, including polymers and coatings, where its properties can enhance durability and performance. The compound's ability to participate in stereospecific reactions also makes it useful in the creation of chiral molecules, which are important in the production of enantiomerically pure substances for medical and industrial applications.
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