N-(Benzo[d][1,3]dioxol-5-yl)-2-chloroacetamide
97%
- Product Code: 50423
CAS:
227199-07-7
| Molecular Weight: | 213.6177 g./mol | Molecular Formula: | C₉H₈ClNO₃ |
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| EC Number: | MDL Number: | MFCD00245737 | |
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| Density: | Storage Condition: | room temperature |
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 pharmaceutical compounds. Its structure, featuring a chloroacetamide group attached to a benzodioxole ring, makes it suitable for further chemical modifications, enabling the creation of molecules with potential therapeutic properties. Additionally, it is employed in research settings for the development of agrochemicals, particularly in the synthesis of herbicides and pesticides, due to its reactive chloro group that can facilitate the formation of biologically active compounds. Its application is also seen in the study of enzyme inhibitors, where it is used to design and test compounds that can modulate enzymatic activity, contributing to advancements in medicinal chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $29.15 |
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N-(Benzo[d][1,3]dioxol-5-yl)-2-chloroacetamide
This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceutical compounds. Its structure, featuring a chloroacetamide group attached to a benzodioxole ring, makes it suitable for further chemical modifications, enabling the creation of molecules with potential therapeutic properties. Additionally, it is employed in research settings for the development of agrochemicals, particularly in the synthesis of herbicides and pesticides, due to its reactive chloro group that can facilitate the formation of biologically active compounds. Its application is also seen in the study of enzyme inhibitors, where it is used to design and test compounds that can modulate enzymatic activity, contributing to advancements in medicinal chemistry.
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