4-Fluoro-2-(trifluoromethyl)benzyl bromide
98%
- Product Code: 118898
Alias:
4-Fluoro-2-(trifluoromethyl)benzyl bromide
CAS:
206860-48-2
| Molecular Weight: | 257.02 g./mol | Molecular Formula: | C₈H₅BrF₄ |
|---|---|---|---|
| EC Number: | 000-000-0 | MDL Number: | MFCD00061176 |
| Melting Point: | Boiling Point: | 141 °C(lit.) | |
| Density: | 1.665 g/mL at 25 °C(lit.) | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile building block for the preparation of more complex molecules. Its benzyl bromide group makes it a valuable reagent for introducing the 4-fluoro-2-(trifluoromethyl)benzyl moiety into various substrates through nucleophilic substitution reactions. It is particularly useful in the development of pharmaceuticals and agrochemicals, where the incorporation of fluorine atoms can enhance the biological activity, metabolic stability, and lipophilicity of the target compounds. Additionally, it serves as an intermediate in the synthesis of specialty chemicals, including dyes, polymers, and materials with unique electronic or optical properties. Its trifluoromethyl group is especially significant in medicinal chemistry, as it often improves binding affinity and selectivity in drug candidates.
Product Specification:
| Test | Specification |
|---|---|
| Purity (Hplc) | 98-100 |
| Purity (Neutralization Titration) | 97.5-102.5 |
| Refractive Index N20/D | 1.481-1.483 |
| Specific Gravity (20/20) | 1.664-1.666 |
| Appearance | Colorless To Yellow Liquid |
| Infrared Spectrometry | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $24.42 |
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| 1.000 | 10-20 days | $57.30 |
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| 5.000 | 10-20 days | $224.49 |
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| 25.000 | 10-20 days | $1,051.99 |
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4-Fluoro-2-(trifluoromethyl)benzyl bromide
This compound is primarily utilized in organic synthesis as a versatile building block for the preparation of more complex molecules. Its benzyl bromide group makes it a valuable reagent for introducing the 4-fluoro-2-(trifluoromethyl)benzyl moiety into various substrates through nucleophilic substitution reactions. It is particularly useful in the development of pharmaceuticals and agrochemicals, where the incorporation of fluorine atoms can enhance the biological activity, metabolic stability, and lipophilicity of the target compounds. Additionally, it serves as an intermediate in the synthesis of specialty chemicals, including dyes, polymers, and materials with unique electronic or optical properties. Its trifluoromethyl group is especially significant in medicinal chemistry, as it often improves binding affinity and selectivity in drug candidates.
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