1,1,1-Trifluoro-4-iodobutane

97%

  • Product Code: 68053
  CAS:    461-17-6
Molecular Weight: 237.99 g./mol Molecular Formula: C₄H₆F₃I
EC Number: MDL Number: MFCD00041543
Melting Point: Boiling Point: 126-127°C(lit.)
Density: 1.850(lit.) Storage Condition: room temperature, dry
Product Description: Used primarily in organic synthesis as a building block for more complex molecules, particularly in the pharmaceutical and agrochemical industries. It serves as a key intermediate in the production of fluorinated compounds, which are valued for their stability and unique chemical properties. The trifluoromethyl group enhances the biological activity of drugs, making it useful in developing active pharmaceutical ingredients. Additionally, it is employed in material science for creating specialty polymers and coatings with improved resistance to heat, chemicals, and weathering. Its iodine atom allows for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical structures.
Product Specification:
Test Specification
APPEARANCE Colorless - Pale reddish yellow Liquid
PURITY 97-100
SPECIFIC GRAVITY 2020 1.8560-1.8600
Refractive index n20D 1.4320-1.4360
Infrared spectrum Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.200 10-20 days ฿290.00
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1.000 10-20 days ฿650.00
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5.000 10-20 days ฿2,250.00
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25.000 10-20 days ฿8,640.00
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1,1,1-Trifluoro-4-iodobutane
Used primarily in organic synthesis as a building block for more complex molecules, particularly in the pharmaceutical and agrochemical industries. It serves as a key intermediate in the production of fluorinated compounds, which are valued for their stability and unique chemical properties. The trifluoromethyl group enhances the biological activity of drugs, making it useful in developing active pharmaceutical ingredients. Additionally, it is employed in material science for creating specialty polymers and coatings with improved resistance to heat, chemicals, and weathering. Its iodine atom allows for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical structures.
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