Methyl2-amino-5-fluoro-3-methylbenzoate

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Reagent Code: #214094
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CAS Number 952479-98-0

science Other reagents with same CAS 952479-98-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 183.18 g/mol
Formula C₉H₁₀FNO₂
badge Registry Numbers
MDL Number MFCD11977398
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system agents. Its structure supports the introduction of fluorine into bioactive molecules, enhancing metabolic stability and binding affinity. Also employed in the preparation of agrochemicals, where the ester and amino functionalities allow for further derivatization into herbicides and fungicides. The compound's aromatic framework with defined substitution pattern makes it valuable in medicinal chemistry for structure-activity relationship (SAR) studies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿16,060.00
inventory 250mg
10-20 days ฿18,320.00
inventory 1g
10-20 days ฿22,900.00
inventory 5g
10-20 days ฿92,180.00

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Methyl2-amino-5-fluoro-3-methylbenzoate
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Used as a key intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system agents. Its structure supports the introduction of fluorine into bioactive molecules, enhancing metabolic stability and binding affinity. Also employed in the preparation of agrochemicals, where the ester and amino functionalities allow for further derivatization into herbicides and fungicides. The compound's aromat

Used as a key intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system agents. Its structure supports the introduction of fluorine into bioactive molecules, enhancing metabolic stability and binding affinity. Also employed in the preparation of agrochemicals, where the ester and amino functionalities allow for further derivatization into herbicides and fungicides. The compound's aromatic framework with defined substitution pattern makes it valuable in medicinal chemistry for structure-activity relationship (SAR) studies.

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