Methyl4-amino-2-fluoro-5-hydroxybenzoate

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Reagent Code: #213673
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CAS Number 2092864-42-9

science Other reagents with same CAS 2092864-42-9

blur_circular Chemical Specifications

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Weight 185.15 g/mol
Formula C₈H₈FNO₃
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of fluorinated pharmaceutical compounds, particularly in the development of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system agents. Its structure supports the introduction of fluorine and hydroxyl functional groups into bioactive molecules, enhancing metabolic stability and binding affinity. Commonly employed in medicinal chemistry for constructing aromatic scaffolds with tailored electronic and steric properties. Also utilized in the preparation of novel analogs for structure-activity relationship (SAR) studies during drug discovery.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,830.00
inventory 250mg
10-20 days ฿11,380.00
inventory 1g
10-20 days ฿22,750.00
inventory 5g
10-20 days ฿74,570.00

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Methyl4-amino-2-fluoro-5-hydroxybenzoate
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Used as a key intermediate in the synthesis of fluorinated pharmaceutical compounds, particularly in the development of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system agents. Its structure supports the introduction of fluorine and hydroxyl functional groups into bioactive molecules, enhancing metabolic stability and binding affinity. Commonly employed in medicinal chemistry for constructing aromatic scaffolds with tailored electronic and steric properties. Also utilized

Used as a key intermediate in the synthesis of fluorinated pharmaceutical compounds, particularly in the development of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system agents. Its structure supports the introduction of fluorine and hydroxyl functional groups into bioactive molecules, enhancing metabolic stability and binding affinity. Commonly employed in medicinal chemistry for constructing aromatic scaffolds with tailored electronic and steric properties. Also utilized in the preparation of novel analogs for structure-activity relationship (SAR) studies during drug discovery.

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