3-[8-(1,4-dioxa-8-azaspiro[4.5]decyl)methyl]benzophenone
97%
- Product Code: 75447
CAS:
898761-26-7
Molecular Weight: | 337.42 g./mol | Molecular Formula: | C₂₁H₂₃NO₃ |
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EC Number: | MDL Number: | MFCD03842177 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | Room temperature, sealed, ventilated |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various complex molecules. Its structure, featuring a benzophenone moiety and a spirocyclic dioxa-aza system, makes it particularly valuable in the development of photolabile protecting groups. These groups are essential in photochemistry and materials science for controlling the release of active compounds under light exposure. Additionally, it finds application in the synthesis of pharmaceuticals, particularly in the creation of compounds with potential therapeutic effects. Its unique architecture also lends itself to the design of advanced materials, such as polymers and coatings, where controlled light-induced reactions are required.
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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3-[8-(1,4-dioxa-8-azaspiro[4.5]decyl)methyl]benzophenone
This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various complex molecules. Its structure, featuring a benzophenone moiety and a spirocyclic dioxa-aza system, makes it particularly valuable in the development of photolabile protecting groups. These groups are essential in photochemistry and materials science for controlling the release of active compounds under light exposure. Additionally, it finds application in the synthesis of pharmaceuticals, particularly in the creation of compounds with potential therapeutic effects. Its unique architecture also lends itself to the design of advanced materials, such as polymers and coatings, where controlled light-induced reactions are required.
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