(Difluoromethyl)triphenylphosphonium bromide

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Reagent Code: #178686
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CAS Number 58310-28-4

science Other reagents with same CAS 58310-28-4

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inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a reagent in organic synthesis, particularly for the introduction of difluoromethyl groups into organic molecules. This phosphonium salt enables the formation of difluoromethylated compounds through Wittig-type reactions, which are valuable in medicinal chemistry for modifying the metabolic stability, lipophilicity, and bioavailability of drug candidates. It is especially useful in the development of fluorinated pharmaceuticals and agrochemicals where the difluoromethylene group acts as a bioisostere for oxygen or carbonyl groups. Its application allows for the efficient and selective construction of complex fluorinated structures under mild conditions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,400.00
inventory 250mg
10-20 days ฿9,140.00
inventory 5g
10-20 days ฿68,190.00
inventory 1g
10-20 days ฿18,250.00

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(Difluoromethyl)triphenylphosphonium bromide
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Used as a reagent in organic synthesis, particularly for the introduction of difluoromethyl groups into organic molecules. This phosphonium salt enables the formation of difluoromethylated compounds through Wittig-type reactions, which are valuable in medicinal chemistry for modifying the metabolic stability, lipophilicity, and bioavailability of drug candidates. It is especially useful in the development of fluorinated pharmaceuticals and agrochemicals where the difluoromethylene group acts as a bioisos

Used as a reagent in organic synthesis, particularly for the introduction of difluoromethyl groups into organic molecules. This phosphonium salt enables the formation of difluoromethylated compounds through Wittig-type reactions, which are valuable in medicinal chemistry for modifying the metabolic stability, lipophilicity, and bioavailability of drug candidates. It is especially useful in the development of fluorinated pharmaceuticals and agrochemicals where the difluoromethylene group acts as a bioisostere for oxygen or carbonyl groups. Its application allows for the efficient and selective construction of complex fluorinated structures under mild conditions.

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