2-(3-fluorobenzyl)isoindoline-1,3-dione
95%
- Product Code: 82322
CAS:
70216-78-3
Molecular Weight: | 255.24 g./mol | Molecular Formula: | C₁₅H₁₀FNO₂ |
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EC Number: | MDL Number: | MFCD05266032 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, where it serves as a versatile intermediate for the development of more complex molecules. Its structure, featuring a fluorobenzyl group attached to an isoindoline-1,3-dione core, makes it valuable in the synthesis of pharmaceuticals, particularly in the creation of compounds with potential therapeutic properties. The fluorine atom enhances the molecule's ability to interact with biological targets, making it useful in drug discovery and development. Additionally, it can be employed in material science for the design of novel organic materials with specific electronic or photophysical properties. Its applications are driven by its ability to undergo various chemical transformations, enabling the creation of diverse derivatives for research and industrial purposes.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | Ft12,605.71 |
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1.000 | 10-20 days | Ft25,211.41 |
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5.000 | 10-20 days | Ft88,239.94 |
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2-(3-fluorobenzyl)isoindoline-1,3-dione
This chemical is primarily utilized in the field of organic synthesis, where it serves as a versatile intermediate for the development of more complex molecules. Its structure, featuring a fluorobenzyl group attached to an isoindoline-1,3-dione core, makes it valuable in the synthesis of pharmaceuticals, particularly in the creation of compounds with potential therapeutic properties. The fluorine atom enhances the molecule's ability to interact with biological targets, making it useful in drug discovery and development. Additionally, it can be employed in material science for the design of novel organic materials with specific electronic or photophysical properties. Its applications are driven by its ability to undergo various chemical transformations, enabling the creation of diverse derivatives for research and industrial purposes.
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