1,1,1,2,2-Pentafluoro-4-iodobutane

99%

Reagent Code: #225194
label
Alias 1H,1H,2H,2H-perfluoroiodobutane; 1,1,1,2,2-pentafluoro-4-iodobutane;
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CAS Number 40723-80-6

science Other reagents with same CAS 40723-80-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 273.97 g/mol
Formula C₄H₄F₅I
badge Registry Numbers
EC Number 255-055-5
MDL Number MFCD00155910
thermostat Physical Properties
Boiling Point 100-101 °C(lit.)
inventory_2 Storage & Handling
Density 1.936 g/mL at 20 °C(lit.)
Storage Room temperature

description Product Description

Used primarily as a fluorinated building block in organic synthesis, especially in pharmaceutical and agrochemical industries. Its iodine functionality allows for coupling reactions, such as cross-coupling or radical reactions, enabling the introduction of a pentafluoropropyl-like group into target molecules. This enhances lipophilicity and metabolic stability in bioactive compounds. Also employed in materials science for modifying surface properties, such as increasing hydrophobicity and chemical resistance in specialty polymers and coatings. Its unique fluorine content makes it valuable in the development of fluorinated reagents and tracers for research applications.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿930.00
25g
10-20 days ฿4,100.00
100g
10-20 days ฿12,970.00
1,1,1,2,2-Pentafluoro-4-iodobutane
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Used primarily as a fluorinated building block in organic synthesis, especially in pharmaceutical and agrochemical industries. Its iodine functionality allows for coupling reactions, such as cross-coupling or radical reactions, enabling the introduction of a pentafluoropropyl-like group into target molecules. This enhances lipophilicity and metabolic stability in bioactive compounds. Also employed in materials science for modifying surface properties, such as increasing hydrophobicity and chemical resist

Used primarily as a fluorinated building block in organic synthesis, especially in pharmaceutical and agrochemical industries. Its iodine functionality allows for coupling reactions, such as cross-coupling or radical reactions, enabling the introduction of a pentafluoropropyl-like group into target molecules. This enhances lipophilicity and metabolic stability in bioactive compounds. Also employed in materials science for modifying surface properties, such as increasing hydrophobicity and chemical resistance in specialty polymers and coatings. Its unique fluorine content makes it valuable in the development of fluorinated reagents and tracers for research applications.

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