Ethyl 3,4-Difluorobenzoate

98%

Reagent Code: #183002
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CAS Number 144267-96-9

science Other reagents with same CAS 144267-96-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 186.16 g/mol
Formula C₉H₈F₂O₂
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of fluorinated drug candidates where the fluorine atoms enhance metabolic stability and bioavailability. Commonly employed in the preparation of active pharmaceutical ingredients (APIs) for central nervous system agents and anti-inflammatory compounds. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and environmental profile. Its ester functionality allows for easy transformation into carboxylic acids, amides, or alcohols during multi-step organic syntheses.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿430.00
inventory 25g
10-20 days ฿1,310.00
inventory 100g
10-20 days ฿5,090.00
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Ethyl 3,4-Difluorobenzoate
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of fluorinated drug candidates where the fluorine atoms enhance metabolic stability and bioavailability. Commonly employed in the preparation of active pharmaceutical ingredients (APIs) for central nervous system agents and anti-inflammatory compounds. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and environmental profile. Its ester functionality allows for easy tra

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of fluorinated drug candidates where the fluorine atoms enhance metabolic stability and bioavailability. Commonly employed in the preparation of active pharmaceutical ingredients (APIs) for central nervous system agents and anti-inflammatory compounds. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and environmental profile. Its ester functionality allows for easy transformation into carboxylic acids, amides, or alcohols during multi-step organic syntheses.

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