Methyl 2,3,4-trifluorobenzoate

98%

Reagent Code: #203133
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CAS Number 773873-68-0

science Other reagents with same CAS 773873-68-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 190.12 g/mol
Formula C₈H₅F₃O₂
badge Registry Numbers
MDL Number MFCD06201866
thermostat Physical Properties
Boiling Point 214.3±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.358±0.06 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals due to its reactive ester group and fluorine substitution pattern. The presence of three fluorine atoms enhances metabolic stability and bioavailability in drug candidates. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies, particularly in the development of central nervous system agents and anti-inflammatory compounds. Also utilized in liquid crystal formulations for display technologies, where fluorinated aromatic cores improve thermal and electro-optical properties. Its ester functionality allows for easy transformation into carboxylic acids, amides, or alcohols, making it a versatile building block in organic synthesis.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿930.00
inventory 5g
10-20 days ฿4,450.00
inventory 25g
10-20 days ฿21,340.00
Methyl 2,3,4-trifluorobenzoate
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Used as a key intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals due to its reactive ester group and fluorine substitution pattern. The presence of three fluorine atoms enhances metabolic stability and bioavailability in drug candidates. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies, particularly in the development of central nervous system agents and anti-inflammatory compounds. Also utilized in liquid crystal formulations for disp

Used as a key intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals due to its reactive ester group and fluorine substitution pattern. The presence of three fluorine atoms enhances metabolic stability and bioavailability in drug candidates. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies, particularly in the development of central nervous system agents and anti-inflammatory compounds. Also utilized in liquid crystal formulations for display technologies, where fluorinated aromatic cores improve thermal and electro-optical properties. Its ester functionality allows for easy transformation into carboxylic acids, amides, or alcohols, making it a versatile building block in organic synthesis.

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