cis-1-Iodo-2-(pentafluoroethyl)cyclohexane

95%

Reagent Code: #200834
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CAS Number 38787-68-7

science Other reagents with same CAS 38787-68-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 328.07 g/mol
Formula C₈H₁₀F₅I
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MDL Number MFCD01862037
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used primarily as a specialized intermediate in organic synthesis, particularly in the preparation of fluorinated pharmaceuticals and agrochemicals. Its unique structure, featuring both an iodo substituent and a pentafluoroethyl group in a cis configuration, allows for selective cross-coupling reactions and functional group transformations. It is especially valuable in the development of bioactive molecules where fluorine substitution enhances metabolic stability, lipophilicity, and binding affinity. The compound also finds use in radiolabeling studies due to the presence of iodine, enabling tracking in biological systems when labeled with radioactive isotopes such as I-125 or I-131.

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿8,800.00
cis-1-Iodo-2-(pentafluoroethyl)cyclohexane
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Used primarily as a specialized intermediate in organic synthesis, particularly in the preparation of fluorinated pharmaceuticals and agrochemicals. Its unique structure, featuring both an iodo substituent and a pentafluoroethyl group in a cis configuration, allows for selective cross-coupling reactions and functional group transformations. It is especially valuable in the development of bioactive molecules where fluorine substitution enhances metabolic stability, lipophilicity, and binding affinity. The

Used primarily as a specialized intermediate in organic synthesis, particularly in the preparation of fluorinated pharmaceuticals and agrochemicals. Its unique structure, featuring both an iodo substituent and a pentafluoroethyl group in a cis configuration, allows for selective cross-coupling reactions and functional group transformations. It is especially valuable in the development of bioactive molecules where fluorine substitution enhances metabolic stability, lipophilicity, and binding affinity. The compound also finds use in radiolabeling studies due to the presence of iodine, enabling tracking in biological systems when labeled with radioactive isotopes such as I-125 or I-131.

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