4-(PEntafluorosulfur)benzylamine

98%

Reagent Code: #227637
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CAS Number 771573-35-4

science Other reagents with same CAS 771573-35-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.2 g/mol
Formula C₇H₈F₅NS
badge Registry Numbers
MDL Number MFCD06213675
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used primarily as a building block in medicinal chemistry, this compound enables the introduction of the pentafluorosulfur (SF5) group into bioactive molecules, enhancing their metabolic stability, lipophilicity, and binding affinity. Its amine functionality allows for easy conjugation to carboxylic acids, carbonyls, or other electrophiles, making it valuable in the synthesis of pharmaceutical candidates and agrochemicals. The strong electron-withdrawing nature of the SF5 group improves the compound’s utility in PET imaging probes due to favorable radiolabeling potential with fluorine-18. It is also explored in materials science for designing high-performance liquid crystals and dielectric compounds owing to the thermal and oxidative stability imparted by the SF5 moiety.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿6,160.00
250mg
10-20 days ฿8,530.00
1g
10-20 days ฿21,620.00
4-(PEntafluorosulfur)benzylamine
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Used primarily as a building block in medicinal chemistry, this compound enables the introduction of the pentafluorosulfur (SF5) group into bioactive molecules, enhancing their metabolic stability, lipophilicity, and binding affinity. Its amine functionality allows for easy conjugation to carboxylic acids, carbonyls, or other electrophiles, making it valuable in the synthesis of pharmaceutical candidates and agrochemicals. The strong electron-withdrawing nature of the SF5 group improves the compound’s ut

Used primarily as a building block in medicinal chemistry, this compound enables the introduction of the pentafluorosulfur (SF5) group into bioactive molecules, enhancing their metabolic stability, lipophilicity, and binding affinity. Its amine functionality allows for easy conjugation to carboxylic acids, carbonyls, or other electrophiles, making it valuable in the synthesis of pharmaceutical candidates and agrochemicals. The strong electron-withdrawing nature of the SF5 group improves the compound’s utility in PET imaging probes due to favorable radiolabeling potential with fluorine-18. It is also explored in materials science for designing high-performance liquid crystals and dielectric compounds owing to the thermal and oxidative stability imparted by the SF5 moiety.

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