2,3,4,5,6-Pentafluorobenzoyl chloride

99%

Reagent Code: #67738
label
Alias 2,3,4,5,6-Pentafluorobenzoyl chloride Pentafluorobenzoyl chloride Pentafluorobenzoyl chloride
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CAS Number 2251-50-5

science Other reagents with same CAS 2251-50-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 230.52 g/mol
Formula C₆F₅COCl
badge Registry Numbers
EC Number 218-842-4
MDL Number MFCD00000657
thermostat Physical Properties
Boiling Point 158-159 °C(lit.)
inventory_2 Storage & Handling
Density 1.601 g/mL at 25 °C(lit.)
Storage 2~8°C, dry, sealed

description Product Description

Used primarily as a reagent in organic synthesis, this compound is highly effective for introducing pentafluorobenzoyl groups into various molecules. It is commonly employed in the preparation of derivatives for analytical purposes, particularly in gas chromatography and mass spectrometry, where it enhances the detectability of compounds due to the electron-withdrawing properties of the pentafluorobenzoyl group. Additionally, it finds application in the development of pharmaceuticals and agrochemicals, where it aids in the modification of molecules to improve their stability, reactivity, or bioavailability. Its use in peptide chemistry is also notable, as it helps in the protection of amino groups during synthesis.

format_list_bulleted Product Specification

Test Parameter Specification
Purity (GC) 98.5-100%
Refractive Index (n20D) 1.452-1.454
Specific Gravity (20°C) 1.666-1.671
Appearance Colorless to light yellow liquid
Infrared Spectrum Conforms to Structure
Proton NMR Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿390.00
inventory 25g
10-20 days ฿2,980.00
inventory 5g
10-20 days ฿1,080.00
inventory 100g
10-20 days ฿9,800.00

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2,3,4,5,6-Pentafluorobenzoyl chloride
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Used primarily as a reagent in organic synthesis, this compound is highly effective for introducing pentafluorobenzoyl groups into various molecules. It is commonly employed in the preparation of derivatives for analytical purposes, particularly in gas chromatography and mass spectrometry, where it enhances the detectability of compounds due to the electron-withdrawing properties of the pentafluorobenzoyl group. Additionally, it finds application in the development of pharmaceuticals and agrochemicals, wher
Used primarily as a reagent in organic synthesis, this compound is highly effective for introducing pentafluorobenzoyl groups into various molecules. It is commonly employed in the preparation of derivatives for analytical purposes, particularly in gas chromatography and mass spectrometry, where it enhances the detectability of compounds due to the electron-withdrawing properties of the pentafluorobenzoyl group. Additionally, it finds application in the development of pharmaceuticals and agrochemicals, where it aids in the modification of molecules to improve their stability, reactivity, or bioavailability. Its use in peptide chemistry is also notable, as it helps in the protection of amino groups during synthesis.
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