3-carboethoxy-4'-[8-(1,4-dioxa-8-azaspiro[4.5]decyl)methyl]benzophenone
97%
- Product Code: 75472
CAS:
898757-68-1
Molecular Weight: | 409.49 g./mol | Molecular Formula: | C₂₄H₂₇NO₅ |
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EC Number: | MDL Number: | MFCD03841677 | |
Melting Point: | Boiling Point: | 562.2℃ at 760 mmHg | |
Density: | 1.25g/ml | Storage Condition: | Room temperature, sealed, ventilated |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, particularly in the development of complex molecular structures. It serves as a key intermediate in the production of specialized organic compounds, including pharmaceuticals and agrochemicals. Its unique structure, featuring a benzophenone core and a dioxa-azaspiro component, makes it valuable for creating compounds with specific biological activities. Additionally, it is employed in research settings for the synthesis of novel materials and as a building block in the design of molecules with potential applications in drug discovery and material science. Its versatility allows it to be used in various chemical reactions, such as cross-coupling and functional group transformations, contributing to advancements in synthetic chemistry.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | €1,533.06 |
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2.000 | 10-20 days | €2,546.92 |
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3-carboethoxy-4'-[8-(1,4-dioxa-8-azaspiro[4.5]decyl)methyl]benzophenone
This chemical is primarily utilized in the field of organic synthesis, particularly in the development of complex molecular structures. It serves as a key intermediate in the production of specialized organic compounds, including pharmaceuticals and agrochemicals. Its unique structure, featuring a benzophenone core and a dioxa-azaspiro component, makes it valuable for creating compounds with specific biological activities. Additionally, it is employed in research settings for the synthesis of novel materials and as a building block in the design of molecules with potential applications in drug discovery and material science. Its versatility allows it to be used in various chemical reactions, such as cross-coupling and functional group transformations, contributing to advancements in synthetic chemistry.
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