Nonitol,1,2,3-trideoxy-4,6:5,7-bis-O-[(4-propylphenyl)methylene]
- Product Code: 84895
CAS:
882073-43-0
| Molecular Weight: | 484.62 g./mol | Molecular Formula: | C₂₉H₄₀O₆ |
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| Density: | Storage Condition: | Room temperature, airtight, dry |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate for the development of more complex molecular structures. Its unique configuration, featuring bis-O-[(4-propylphenyl)methylene] groups, makes it particularly valuable in the synthesis of specialized polymers and resins. These materials are often employed in high-performance coatings, adhesives, and composites, where enhanced thermal stability and mechanical properties are required. Additionally, its application extends to the pharmaceutical industry, where it is used in the preparation of certain drug candidates, leveraging its structural complexity to achieve specific biological activities. The chemical's ability to act as a chiral building block also makes it useful in the production of optically active compounds, which are critical in the development of enantiomerically pure pharmaceuticals.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | €2,268.85 |
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Nonitol,1,2,3-trideoxy-4,6:5,7-bis-O-[(4-propylphenyl)methylene]
This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate for the development of more complex molecular structures. Its unique configuration, featuring bis-O-[(4-propylphenyl)methylene] groups, makes it particularly valuable in the synthesis of specialized polymers and resins. These materials are often employed in high-performance coatings, adhesives, and composites, where enhanced thermal stability and mechanical properties are required. Additionally, its application extends to the pharmaceutical industry, where it is used in the preparation of certain drug candidates, leveraging its structural complexity to achieve specific biological activities. The chemical's ability to act as a chiral building block also makes it useful in the production of optically active compounds, which are critical in the development of enantiomerically pure pharmaceuticals.
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