Ethyl hexafluoroglutaryl chloride

97%, used for GC derivatization

Reagent Code: #182137
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CAS Number 18381-53-8

science Other reagents with same CAS 18381-53-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 286.56 g/mol
Formula C₇H₅ClF₆O₃
badge Registry Numbers
MDL Number MFCD00054671
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Used primarily as a fluorinated building block in organic synthesis, especially in the development of pharmaceuticals and agrochemicals. Its high fluorine content enhances metabolic stability and lipophilicity in bioactive molecules, making it valuable in designing drugs with improved bioavailability and target specificity. It is also employed in the synthesis of specialty polymers and functional materials where thermal and chemical resistance are required. Due to the reactive acid chloride group, it readily forms amides, esters, and other derivatives under mild conditions, enabling efficient incorporation into complex molecular architectures. Its application is particularly notable in medicinal chemistry for creating fluorinated analogs of natural compounds.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,250.00
inventory 1g
10-20 days ฿9,140.00
inventory 5g
10-20 days ฿39,590.00
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Ethyl hexafluoroglutaryl chloride
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Used primarily as a fluorinated building block in organic synthesis, especially in the development of pharmaceuticals and agrochemicals. Its high fluorine content enhances metabolic stability and lipophilicity in bioactive molecules, making it valuable in designing drugs with improved bioavailability and target specificity. It is also employed in the synthesis of specialty polymers and functional materials where thermal and chemical resistance are required. Due to the reactive acid chloride group, it rea

Used primarily as a fluorinated building block in organic synthesis, especially in the development of pharmaceuticals and agrochemicals. Its high fluorine content enhances metabolic stability and lipophilicity in bioactive molecules, making it valuable in designing drugs with improved bioavailability and target specificity. It is also employed in the synthesis of specialty polymers and functional materials where thermal and chemical resistance are required. Due to the reactive acid chloride group, it readily forms amides, esters, and other derivatives under mild conditions, enabling efficient incorporation into complex molecular architectures. Its application is particularly notable in medicinal chemistry for creating fluorinated analogs of natural compounds.

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