4-(Trifluoromethyl)benzyl bromide

98%

  • Product Code: 118661
  Alias:    4-(Trifluoromethyl)benzyl bromide; 1-Bromo-trifluoro-p-xylene
  CAS:    402-49-3
Molecular Weight: 239.03 g./mol Molecular Formula: C₈H₆BrF₃
EC Number: 206-947-8 MDL Number: MFCD00000403
Melting Point: 29-33 °C(lit.) Boiling Point: 65-69 °C5 mm Hg(lit.)
Density: 1.546 g/mL at 25 °C(lit.) Storage Condition: room temperature
Product Description: 4-(Trifluoromethyl)benzyl bromide is widely used as a versatile intermediate in organic synthesis. It is particularly valuable in the preparation of pharmaceuticals, agrochemicals, and specialty chemicals. The trifluoromethyl group enhances the biological activity and metabolic stability of compounds, making it a key building block in drug discovery. It is also employed in the synthesis of liquid crystals and advanced materials due to its unique electronic properties. Additionally, it serves as a reagent in cross-coupling reactions and other transformations to introduce the benzyl bromide moiety into target molecules.
Product Specification:
Test Specification
Melting Point 30-34
Purity (GC) 98-100%
Appearance White To Light Yellow Solid
Infrared Spectrum Conforms To Structure
Note This Product Is Low Melting Point Solid, May Change State In Different Environments
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿290.00
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5.000 10-20 days ฿450.00
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25.000 10-20 days ฿1,190.00
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100.000 10-20 days ฿4,240.00
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500.000 10-20 days ฿20,040.00
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4-(Trifluoromethyl)benzyl bromide
4-(Trifluoromethyl)benzyl bromide is widely used as a versatile intermediate in organic synthesis. It is particularly valuable in the preparation of pharmaceuticals, agrochemicals, and specialty chemicals. The trifluoromethyl group enhances the biological activity and metabolic stability of compounds, making it a key building block in drug discovery. It is also employed in the synthesis of liquid crystals and advanced materials due to its unique electronic properties. Additionally, it serves as a reagent in cross-coupling reactions and other transformations to introduce the benzyl bromide moiety into target molecules.
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