Methyl 2,4,5-triamino-3-fluorobenzoate

95%

Reagent Code: #209533
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CAS Number 918321-27-4

science Other reagents with same CAS 918321-27-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 199.182 g/mol
Formula C₈H₁₀FN₃O₂
badge Registry Numbers
MDL Number MFCD20725583
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used in the synthesis of fluorinated pharmaceutical intermediates, particularly in the development of kinase inhibitors and antiviral agents. Its structure supports the formation of hydrogen bonds and dipole interactions, enhancing binding affinity in drug-receptor interactions. Also employed in the preparation of specialty dyes and fluorescent probes due to its electron-rich aromatic system and amino groups that facilitate conjugation. Commonly utilized in research settings for building blocks in heterocyclic chemistry, especially in the design of novel bioactive molecules.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,440.00
inventory 250mg
10-20 days ฿4,040.00
inventory 1g
10-20 days ฿8,060.00
Methyl 2,4,5-triamino-3-fluorobenzoate
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Used in the synthesis of fluorinated pharmaceutical intermediates, particularly in the development of kinase inhibitors and antiviral agents. Its structure supports the formation of hydrogen bonds and dipole interactions, enhancing binding affinity in drug-receptor interactions. Also employed in the preparation of specialty dyes and fluorescent probes due to its electron-rich aromatic system and amino groups that facilitate conjugation. Commonly utilized in research settings for building blocks in hetero

Used in the synthesis of fluorinated pharmaceutical intermediates, particularly in the development of kinase inhibitors and antiviral agents. Its structure supports the formation of hydrogen bonds and dipole interactions, enhancing binding affinity in drug-receptor interactions. Also employed in the preparation of specialty dyes and fluorescent probes due to its electron-rich aromatic system and amino groups that facilitate conjugation. Commonly utilized in research settings for building blocks in heterocyclic chemistry, especially in the design of novel bioactive molecules.

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