ethyl 6-[3-[8-(1,4-dioxa-8-azaspiro[4.5]decyl)methyl]phenyl]-6-oxohexanoate
97%
- Product Code: 75961
CAS:
898762-64-6
Molecular Weight: | 389.5 g./mol | Molecular Formula: | C₂₂H₃₁NO₅ |
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EC Number: | MDL Number: | MFCD03842229 | |
Melting Point: | Boiling Point: | 520℃ at 760 mmHg | |
Density: | 1.17g/ml | Storage Condition: | Room temperature, sealed, ventilated |
Product Description:
This chemical is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting neurological and cardiovascular disorders. Its structure, featuring a spirocyclic dioxa-aza system, makes it valuable for developing molecules with enhanced binding affinity and selectivity towards specific receptors or enzymes. Researchers often employ it in the design and optimization of drugs aimed at modulating neurotransmitter systems or improving metabolic pathways. Additionally, its ester functionality allows for further chemical modifications, enabling the creation of prodrugs or derivatives with improved pharmacokinetic properties.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | ฿56,240.00 |
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2.000 | 10-20 days | ฿93,420.00 |
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ethyl 6-[3-[8-(1,4-dioxa-8-azaspiro[4.5]decyl)methyl]phenyl]-6-oxohexanoate
This chemical is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting neurological and cardiovascular disorders. Its structure, featuring a spirocyclic dioxa-aza system, makes it valuable for developing molecules with enhanced binding affinity and selectivity towards specific receptors or enzymes. Researchers often employ it in the design and optimization of drugs aimed at modulating neurotransmitter systems or improving metabolic pathways. Additionally, its ester functionality allows for further chemical modifications, enabling the creation of prodrugs or derivatives with improved pharmacokinetic properties.
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