8-Phenyl-1-thia-4-azaspiro[4.5]decane-3-carboxylic acid
95%
- Product Code: 75801
CAS:
367928-68-5
| Molecular Weight: | 277.38 g./mol | Molecular Formula: | C₁₅H₁₉NO₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02648392 | |
| Melting Point: | 207℃ | Boiling Point: | |
| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its unique spirocyclic structure makes it valuable for developing compounds with potential therapeutic effects, particularly in the design of drugs targeting neurological disorders. Researchers often explore its derivatives for their ability to modulate specific enzymes or receptors in the central nervous system, making it a promising candidate for the development of treatments for conditions such as anxiety, depression, or neurodegenerative diseases. Additionally, its structural features are leveraged in the creation of novel antibiotics, as it can serve as a scaffold for molecules that disrupt bacterial cell wall synthesis or other critical microbial processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿27,873.00 |
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| 5.000 | 10-20 days | ฿64,062.00 |
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8-Phenyl-1-thia-4-azaspiro[4.5]decane-3-carboxylic acid
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its unique spirocyclic structure makes it valuable for developing compounds with potential therapeutic effects, particularly in the design of drugs targeting neurological disorders. Researchers often explore its derivatives for their ability to modulate specific enzymes or receptors in the central nervous system, making it a promising candidate for the development of treatments for conditions such as anxiety, depression, or neurodegenerative diseases. Additionally, its structural features are leveraged in the creation of novel antibiotics, as it can serve as a scaffold for molecules that disrupt bacterial cell wall synthesis or other critical microbial processes.
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