(11bR)-3,5-Dihydro-spiro[4H-cyclohepta[2,1-a:3,4-a']dinaphthalene-4,1'-[2,4]cyclopentadiene]-2,6-diol
98%
- Product Code: 70124
CAS:
1417714-09-0
Molecular Weight: | 376.4 g./mol | Molecular Formula: | C₂₇H₂₀O₂ |
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EC Number: | MDL Number: | ||
Melting Point: | Boiling Point: | 612.9±55.0 °C | |
Density: | 1.37±0.1 g/cm3 | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry due to its unique structural properties. It serves as a key intermediate in the synthesis of complex pharmaceutical agents, particularly those targeting neurological disorders. The compound's rigid spirocyclic framework makes it an ideal candidate for developing drugs that require high specificity and stability. Researchers are exploring its potential in creating novel therapeutics for conditions like Parkinson's disease and Alzheimer's, as it can interact with specific receptors in the brain. Additionally, its diol groups provide reactive sites for further chemical modifications, enabling the development of derivatives with enhanced pharmacological activity. Its application in drug discovery highlights its importance in advancing treatments for challenging medical conditions.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.010 | 10-20 days | ฿9,900.00 |
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0.050 | 10-20 days | ฿39,528.00 |
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(11bR)-3,5-Dihydro-spiro[4H-cyclohepta[2,1-a:3,4-a']dinaphthalene-4,1'-[2,4]cyclopentadiene]-2,6-diol
This compound is primarily utilized in the field of medicinal chemistry due to its unique structural properties. It serves as a key intermediate in the synthesis of complex pharmaceutical agents, particularly those targeting neurological disorders. The compound's rigid spirocyclic framework makes it an ideal candidate for developing drugs that require high specificity and stability. Researchers are exploring its potential in creating novel therapeutics for conditions like Parkinson's disease and Alzheimer's, as it can interact with specific receptors in the brain. Additionally, its diol groups provide reactive sites for further chemical modifications, enabling the development of derivatives with enhanced pharmacological activity. Its application in drug discovery highlights its importance in advancing treatments for challenging medical conditions.
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