1-(4-Chloro-2-(3-methyl-1H-pyrazol-1-yl)phenyl)-2,2,2-trifluoroethanone
97%
- Product Code: 114415
CAS:
1125828-30-9
| Molecular Weight: | 288.65 g./mol | Molecular Formula: | C₁₂H₈ClF₃N₂O |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD14706009 | |
| Melting Point: | Boiling Point: | 365.4±42.0°C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
This chemical is primarily utilized in the field of agrochemical research and development. It serves as a key intermediate in the synthesis of various herbicides and pesticides, particularly those designed to target specific weed species without harming crops. Its unique structure allows for the creation of compounds that inhibit essential enzymes in weeds, leading to their controlled growth and eventual elimination. Additionally, it is explored in pharmaceutical research for its potential role in developing bioactive molecules, particularly in the design of enzyme inhibitors or receptor modulators. Its trifluoroethanone moiety contributes to its stability and reactivity, making it a valuable building block in organic synthesis.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿441.00 |
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| 1.000 | 10-20 days | ฿1,125.00 |
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| 5.000 | 10-20 days | ฿3,960.00 |
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1-(4-Chloro-2-(3-methyl-1H-pyrazol-1-yl)phenyl)-2,2,2-trifluoroethanone
This chemical is primarily utilized in the field of agrochemical research and development. It serves as a key intermediate in the synthesis of various herbicides and pesticides, particularly those designed to target specific weed species without harming crops. Its unique structure allows for the creation of compounds that inhibit essential enzymes in weeds, leading to their controlled growth and eventual elimination. Additionally, it is explored in pharmaceutical research for its potential role in developing bioactive molecules, particularly in the design of enzyme inhibitors or receptor modulators. Its trifluoroethanone moiety contributes to its stability and reactivity, making it a valuable building block in organic synthesis.
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