5-Amino-4-fluoro-2-methyl-benzoic acid methyl ester

≥95%

Reagent Code: #133408
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CAS Number 1567119-84-9

science Other reagents with same CAS 1567119-84-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 183.1796 g/mol
Formula C₉H₁₀FNO₂
badge Registry Numbers
MDL Number MFCD26862940
thermostat Physical Properties
Boiling Point 277.5±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.220±0.06 g/cm3(Predicted)
Storage Room temperature, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of fluorinated pharmaceutical compounds, particularly in the development of selective kinase inhibitors. Its structure supports the creation of bioactive molecules with improved metabolic stability and binding affinity. Commonly employed in medicinal chemistry for constructing drug candidates targeting inflammatory diseases and certain cancers. The ester group facilitates further chemical modifications, making it valuable in multi-step organic syntheses.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿12,800.00
250mg
10-20 days ฿16,000.00
500mg
10-20 days ฿22,400.00
1g
10-20 days ฿32,000.00
5g
10-20 days ฿112,000.00
5-Amino-4-fluoro-2-methyl-benzoic acid methyl ester
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Used as a key intermediate in the synthesis of fluorinated pharmaceutical compounds, particularly in the development of selective kinase inhibitors. Its structure supports the creation of bioactive molecules with improved metabolic stability and binding affinity. Commonly employed in medicinal chemistry for constructing drug candidates targeting inflammatory diseases and certain cancers. The ester group facilitates further chemical modifications, making it valuable in multi-step organic syntheses.

Used as a key intermediate in the synthesis of fluorinated pharmaceutical compounds, particularly in the development of selective kinase inhibitors. Its structure supports the creation of bioactive molecules with improved metabolic stability and binding affinity. Commonly employed in medicinal chemistry for constructing drug candidates targeting inflammatory diseases and certain cancers. The ester group facilitates further chemical modifications, making it valuable in multi-step organic syntheses.

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