4-Amino-2-fluorobenzoic acid

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Reagent Code: #134910
label
Alias 4-amino-2-fluorobenzoic acid
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CAS Number 446-31-1

science Other reagents with same CAS 446-31-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 155.13 g/mol
Formula C₇H₆FNO₂
badge Registry Numbers
MDL Number MFCD01569397
thermostat Physical Properties
Melting Point 210 °C ( dec.)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and central nervous system drugs. Its structure allows for selective binding in biologically active molecules, making it valuable in medicinal chemistry. Also employed in the preparation of fluorinated analogs to enhance metabolic stability and bioavailability in drug candidates. Additionally, it serves as a building block in the creation of specialty polymers and agrochemicals where fluorine substitution improves performance.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿290.00
inventory 1g
10-20 days ฿350.00
inventory 5g
10-20 days ฿900.00
inventory 25g
10-20 days ฿3,900.00
inventory 100g
10-20 days ฿15,300.00

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4-Amino-2-fluorobenzoic acid
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and central nervous system drugs. Its structure allows for selective binding in biologically active molecules, making it valuable in medicinal chemistry. Also employed in the preparation of fluorinated analogs to enhance metabolic stability and bioavailability in drug candidates. Additionally, it serves as a building block in the creation of specialty polymers and agrochemicals where fluorine

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and central nervous system drugs. Its structure allows for selective binding in biologically active molecules, making it valuable in medicinal chemistry. Also employed in the preparation of fluorinated analogs to enhance metabolic stability and bioavailability in drug candidates. Additionally, it serves as a building block in the creation of specialty polymers and agrochemicals where fluorine substitution improves performance.

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