4'-[8-(1,4-dioxa-8-azaspiro[4.5]decyl)methyl]-4-thiomethyl benzophenone
97%
- Product Code: 75530
CAS:
898757-74-9
Molecular Weight: | 383.51 g./mol | Molecular Formula: | C₂₂H₂₅NO₃S |
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EC Number: | MDL Number: | MFCD03841680 | |
Melting Point: | Boiling Point: | 539.6℃ at 760 mmHg | |
Density: | 1.25g/ml | Storage Condition: | Room temperature, sealed, ventilated |
Product Description:
This compound is primarily utilized in the field of organic synthesis, particularly as a key intermediate in the development of complex molecules. Its structure, featuring a benzophenone core with a thiomethyl group and a dioxa-azaspiro moiety, makes it valuable for constructing pharmacologically active compounds. It is often employed in the synthesis of drug candidates, especially those targeting neurological disorders, due to its potential to interact with biological systems. Additionally, its unique spirocyclic structure is exploited in materials science for designing advanced polymers and coatings with specific optical or mechanical properties. The compound’s versatility also extends to its use in photochemical studies, where it serves as a photosensitive agent in research applications.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | ฿58,110.00 |
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2.000 | 10-20 days | ฿96,540.00 |
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4'-[8-(1,4-dioxa-8-azaspiro[4.5]decyl)methyl]-4-thiomethyl benzophenone
This compound is primarily utilized in the field of organic synthesis, particularly as a key intermediate in the development of complex molecules. Its structure, featuring a benzophenone core with a thiomethyl group and a dioxa-azaspiro moiety, makes it valuable for constructing pharmacologically active compounds. It is often employed in the synthesis of drug candidates, especially those targeting neurological disorders, due to its potential to interact with biological systems. Additionally, its unique spirocyclic structure is exploited in materials science for designing advanced polymers and coatings with specific optical or mechanical properties. The compound’s versatility also extends to its use in photochemical studies, where it serves as a photosensitive agent in research applications.
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