1-(4-Bromo-2-(trifluoromethyl)phenyl)thiourea
97%
- Product Code: 142379
Alias:
[4-Bromo-2-(trifluoromethyl)phenyl]thiourea; 4-Bromo-2-trifluoromethyl-phenylthiourea
CAS:
208186-71-4
| Molecular Weight: | 299.11 g./mol | Molecular Formula: | C₈H₆BrF₃N₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00041177 | |
| Melting Point: | 176-181 °C | Boiling Point: | |
| Density: | Storage Condition: | Room temperature, seal, dry |
Product Description:
Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules with potential antitumor and antimicrobial properties. It serves as a building block in medicinal chemistry for constructing heterocyclic compounds that exhibit enzyme inhibitory activity. Also employed in agrochemical research for designing novel pesticides and herbicides due to its halogenated aromatic structure, which can enhance binding affinity and metabolic stability. Its thiourea functional group allows for hydrogen bonding interactions, making it valuable in the design of sensors and molecular recognition systems.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White to Brown Powder, Crystals or Crystalline Powder and/or Chunks |
| Purity (%) | 96.5-100 |
| Infrared Spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $50.85 |
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| 1.000 | 10-20 days | $168.13 |
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| 5.000 | 10-20 days | $824.04 |
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| 25.000 | 10-20 days | $2,485.63 |
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1-(4-Bromo-2-(trifluoromethyl)phenyl)thiourea
Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules with potential antitumor and antimicrobial properties. It serves as a building block in medicinal chemistry for constructing heterocyclic compounds that exhibit enzyme inhibitory activity. Also employed in agrochemical research for designing novel pesticides and herbicides due to its halogenated aromatic structure, which can enhance binding affinity and metabolic stability. Its thiourea functional group allows for hydrogen bonding interactions, making it valuable in the design of sensors and molecular recognition systems.
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