2-Amino-4-chloro-5-fluorobenzoic acid

98%

Reagent Code: #135734
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CAS Number 108288-16-0

science Other reagents with same CAS 108288-16-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 189.57 g/mol
Formula C₇H₅ClFNO₂
thermostat Physical Properties
Boiling Point 350.1°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and central nervous system agents. It serves as a building block for fluorinated and chlorinated aromatic compounds, enhancing metabolic stability and bioavailability in drug candidates. Also employed in the preparation of agrochemicals and specialty organic materials where halogen and amino functionalities are required for activity. Its structure allows for further functionalization via amide coupling or diazotization, making it valuable in medicinal chemistry research.

format_list_bulleted Product Specification

Test Parameter Specification
APPEARANCE Gray to pink solid
Purity (%) 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿990.00
250mg
10-20 days ฿1,540.00
1g
10-20 days ฿3,160.00
5g
10-20 days ฿11,920.00
2-Amino-4-chloro-5-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 agents. It serves as a building block for fluorinated and chlorinated aromatic compounds, enhancing metabolic stability and bioavailability in drug candidates. Also employed in the preparation of agrochemicals and specialty organic materials where halogen and amino functionalities are required for activity. Its structure allows for further functionalization via amid

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and central nervous system agents. It serves as a building block for fluorinated and chlorinated aromatic compounds, enhancing metabolic stability and bioavailability in drug candidates. Also employed in the preparation of agrochemicals and specialty organic materials where halogen and amino functionalities are required for activity. Its structure allows for further functionalization via amide coupling or diazotization, making it valuable in medicinal chemistry research.

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