Triethylamine trihydrofluoride

99%

Reagent Code: #238116
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CAS Number 73602-61-6

science Other reagents with same CAS 73602-61-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 161.21 g/mol
Formula C₆H₁₅N·₃HF
badge Registry Numbers
EC Number 277-550-5
MDL Number MFCD00043294
thermostat Physical Properties
Melting Point -29-27 °C
Boiling Point 70 °C/15 mm Hg(lit.)
inventory_2 Storage & Handling
Density 0.989 g/mL at 25 °C(lit.)
Storage Room temperature, inert gas

description Product Description

Widely used as a selective fluorinating agent in organic synthesis, particularly in the preparation of fluorinated pharmaceuticals and agrochemicals. It is effective for converting alcohols to alkyl fluorides and for replacing hydroxyl groups with fluorine in sugar derivatives and nucleosides, which is valuable in medicinal chemistry. Its mild reactivity allows for good functional group tolerance, making it suitable for complex molecules. Also employed in deprotection steps in peptide and oligonucleotide synthesis due to its ability to cleave certain protecting groups under controlled conditions. Additionally, it serves as a fluorine source in industrial processes requiring safe and stable handling of hydrogen fluoride equivalents.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿400.00
inventory 25g
10-20 days ฿680.00
inventory 100g
10-20 days ฿1,340.00

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Triethylamine trihydrofluoride
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Widely used as a selective fluorinating agent in organic synthesis, particularly in the preparation of fluorinated pharmaceuticals and agrochemicals. It is effective for converting alcohols to alkyl fluorides and for replacing hydroxyl groups with fluorine in sugar derivatives and nucleosides, which is valuable in medicinal chemistry. Its mild reactivity allows for good functional group tolerance, making it suitable for complex molecules. Also employed in deprotection steps in peptide and oligonucleotide

Widely used as a selective fluorinating agent in organic synthesis, particularly in the preparation of fluorinated pharmaceuticals and agrochemicals. It is effective for converting alcohols to alkyl fluorides and for replacing hydroxyl groups with fluorine in sugar derivatives and nucleosides, which is valuable in medicinal chemistry. Its mild reactivity allows for good functional group tolerance, making it suitable for complex molecules. Also employed in deprotection steps in peptide and oligonucleotide synthesis due to its ability to cleave certain protecting groups under controlled conditions. Additionally, it serves as a fluorine source in industrial processes requiring safe and stable handling of hydrogen fluoride equivalents.

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