sodium 2,3-difluorobenzoate

≥95%

Reagent Code: #234694
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CAS Number 1604819-08-0

science Other reagents with same CAS 1604819-08-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 180.08 g/mol
Formula C₇H₃F₂NaO₂
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a fluorinated building block in pharmaceutical synthesis, particularly in the development of fluorine-containing active pharmaceutical ingredients (APIs) where enhanced metabolic stability and bioavailability are desired. Its difluorinated aromatic structure makes it valuable in medicinal chemistry for modulating the electronic and steric properties of drug candidates. Also employed in agrochemical research for designing novel pesticides and herbicides with improved environmental resistance. Additionally, it serves as a reagent or intermediate in specialty organic reactions, including cross-coupling and nucleophilic aromatic substitution, benefiting from the activating effect of fluorine substituents.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,950.00
inventory 5g
10-20 days ฿30,090.00
inventory 1g
10-20 days ฿7,940.00
sodium 2,3-difluorobenzoate
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Used as a fluorinated building block in pharmaceutical synthesis, particularly in the development of fluorine-containing active pharmaceutical ingredients (APIs) where enhanced metabolic stability and bioavailability are desired. Its difluorinated aromatic structure makes it valuable in medicinal chemistry for modulating the electronic and steric properties of drug candidates. Also employed in agrochemical research for designing novel pesticides and herbicides with improved environmental resistance. Addi

Used as a fluorinated building block in pharmaceutical synthesis, particularly in the development of fluorine-containing active pharmaceutical ingredients (APIs) where enhanced metabolic stability and bioavailability are desired. Its difluorinated aromatic structure makes it valuable in medicinal chemistry for modulating the electronic and steric properties of drug candidates. Also employed in agrochemical research for designing novel pesticides and herbicides with improved environmental resistance. Additionally, it serves as a reagent or intermediate in specialty organic reactions, including cross-coupling and nucleophilic aromatic substitution, benefiting from the activating effect of fluorine substituents.

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