4-Amino-2-fluorophenol

>98.0%(GC)

Reagent Code: #134995
label
Alias 3-Fluoro-4-hydroxyaniline
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CAS Number 399-96-2

science Other reagents with same CAS 399-96-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 127.12 g/mol
Formula C₆H₆FNO
badge Registry Numbers
MDL Number MFCD00671760
thermostat Physical Properties
Melting Point 170-172°C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system agents. It also serves in the preparation of agrochemicals, dyes, and fluorescent probes due to its reactive amino and hydroxyl groups. Its fluorinated aromatic structure enhances binding selectivity in drug molecules, making it valuable in medicinal chemistry for optimizing pharmacokinetic properties.

format_list_bulleted Product Specification

Test Parameter Specification
Purity (GC)`,`MAX: 98-100
Purity (Nonaqueous Titration)`,`MAX: 98-100
INFRARED SPECTROMETRY`,`MAX: Conforms to Structure

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿270.00
5g
10-20 days ฿1,090.00
25g
10-20 days ฿5,290.00
4-Amino-2-fluorophenol
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system agents. It also serves in the preparation of agrochemicals, dyes, and fluorescent probes due to its reactive amino and hydroxyl groups. Its fluorinated aromatic structure enhances binding selectivity in drug molecules, making it valuable in medicinal chemistry for optimizing pharmacokinetic properties.

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system agents. It also serves in the preparation of agrochemicals, dyes, and fluorescent probes due to its reactive amino and hydroxyl groups. Its fluorinated aromatic structure enhances binding selectivity in drug molecules, making it valuable in medicinal chemistry for optimizing pharmacokinetic properties.

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