Sodium 2,3,4,5-tetrafluorobenzoate

>95%

Reagent Code: #57818
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CAS Number 67852-79-3

science Other reagents with same CAS 67852-79-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 216.07 g/mol
Formula C₇HF₄NaO₂
thermostat Physical Properties
Boiling Point 239.2ºC at 760 mmHg
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in the field of organic synthesis as a versatile building block for the preparation of more complex fluorinated aromatic compounds. Its fluorine atoms make it highly reactive, enabling it to participate in various coupling reactions, such as Suzuki or Sonogashira couplings, which are essential in the development of pharmaceuticals and agrochemicals. Additionally, it serves as a key intermediate in the synthesis of liquid crystals and advanced materials, where the introduction of fluorine atoms enhances thermal stability and chemical resistance. Its unique structure also makes it valuable in the design of active pharmaceutical ingredients (APIs), particularly in the development of drugs targeting specific biological pathways.

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Test Parameter Specification
Purity 95-100%
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 10 g
10-20 days ฿1,440.00
inventory 1 g
10-20 days ฿300.00
inventory 5 g
10-20 days ฿730.00
inventory 50 g
10-20 days ฿5,040.00

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Sodium 2,3,4,5-tetrafluorobenzoate
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This compound is primarily utilized in the field of organic synthesis as a versatile building block for the preparation of more complex fluorinated aromatic compounds. Its fluorine atoms make it highly reactive, enabling it to participate in various coupling reactions, such as Suzuki or Sonogashira couplings, which are essential in the development of pharmaceuticals and agrochemicals. Additionally, it serves as a key intermediate in the synthesis of liquid crystals and advanced materials, where the intro

This compound is primarily utilized in the field of organic synthesis as a versatile building block for the preparation of more complex fluorinated aromatic compounds. Its fluorine atoms make it highly reactive, enabling it to participate in various coupling reactions, such as Suzuki or Sonogashira couplings, which are essential in the development of pharmaceuticals and agrochemicals. Additionally, it serves as a key intermediate in the synthesis of liquid crystals and advanced materials, where the introduction of fluorine atoms enhances thermal stability and chemical resistance. Its unique structure also makes it valuable in the design of active pharmaceutical ingredients (APIs), particularly in the development of drugs targeting specific biological pathways.

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