3-[8-(1,4-dioxa-8-azaspiro[4.5]decyl)methyl]-3'-methoxy benzophenone
97%
- Product Code: 75452
CAS:
898761-41-6
| Molecular Weight: | 367.45 g./mol | Molecular Formula: | C₂₂H₂₅NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03842182 | |
| Melting Point: | Boiling Point: | 529.1℃ at 760 mmHg | |
| Density: | 1.23g/ml | Storage Condition: | Room temperature, sealed, ventilated |
Product Description:
This chemical is primarily used in the field of organic synthesis, particularly in the development of photolabile protecting groups. It is employed in the protection of functional groups during complex chemical reactions, especially in peptide and nucleotide synthesis, where selective deprotection is required. The compound’s structure allows it to be cleaved under specific light conditions, making it valuable in photochemistry and light-sensitive applications. Additionally, it finds use in material science for the development of light-responsive materials and coatings. Its role in research and development of advanced pharmaceutical compounds is also notable, as it aids in the controlled release of active ingredients under targeted conditions.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿59,360.00 |
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| 2.000 | 10-20 days | ฿98,610.00 |
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3-[8-(1,4-dioxa-8-azaspiro[4.5]decyl)methyl]-3'-methoxy benzophenone
This chemical is primarily used in the field of organic synthesis, particularly in the development of photolabile protecting groups. It is employed in the protection of functional groups during complex chemical reactions, especially in peptide and nucleotide synthesis, where selective deprotection is required. The compound’s structure allows it to be cleaved under specific light conditions, making it valuable in photochemistry and light-sensitive applications. Additionally, it finds use in material science for the development of light-responsive materials and coatings. Its role in research and development of advanced pharmaceutical compounds is also notable, as it aids in the controlled release of active ingredients under targeted conditions.
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