1-(1-Bromoethyl)-2-(difluoromethoxy)benzene
95%
- Product Code: 39107
CAS:
1094272-74-8
| Molecular Weight: | 251.0680 g./mol | Molecular Formula: | C₉H₉BrF₂O |
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| Density: | Storage Condition: | room temperature |
Product Description:
1-(1-Bromoethyl)-2-(difluoromethoxy)benzene is primarily utilized in organic synthesis as a key intermediate in the production of more complex chemical compounds. Its structure, featuring both a bromoethyl group and a difluoromethoxy group, makes it valuable for introducing these functional groups into target molecules during chemical reactions. It is often employed in the development of pharmaceuticals, particularly in the synthesis of active pharmaceutical ingredients (APIs) where the difluoromethoxy moiety can enhance metabolic stability and bioavailability. Additionally, this compound is used in agrochemical research for the creation of novel pesticides or herbicides, leveraging its unique chemical properties to improve efficacy and selectivity. Its role in cross-coupling reactions, such as Suzuki or Heck reactions, further highlights its importance in constructing aromatic systems with specific functional group patterns.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿8,244.00 |
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1-(1-Bromoethyl)-2-(difluoromethoxy)benzene
1-(1-Bromoethyl)-2-(difluoromethoxy)benzene is primarily utilized in organic synthesis as a key intermediate in the production of more complex chemical compounds. Its structure, featuring both a bromoethyl group and a difluoromethoxy group, makes it valuable for introducing these functional groups into target molecules during chemical reactions. It is often employed in the development of pharmaceuticals, particularly in the synthesis of active pharmaceutical ingredients (APIs) where the difluoromethoxy moiety can enhance metabolic stability and bioavailability. Additionally, this compound is used in agrochemical research for the creation of novel pesticides or herbicides, leveraging its unique chemical properties to improve efficacy and selectivity. Its role in cross-coupling reactions, such as Suzuki or Heck reactions, further highlights its importance in constructing aromatic systems with specific functional group patterns.
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