4-Fluoro-3-methoxyphenylacetic acid
97%
- Product Code: 187738
CAS:
946713-86-6
Molecular Weight: | 184.16 g./mol | Molecular Formula: | C₉H₉FO₃ |
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EC Number: | MDL Number: | MFCD08146650 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | Room temperature, dry |
Product Description:
Used in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs) for central nervous system (CNS) drugs. It serves as a building block in the preparation of fluorinated analogs of bioactive molecules, where the fluorine atom enhances metabolic stability and membrane permeability. Commonly employed in the production of selective serotonin reuptake inhibitors (SSRIs) and related antidepressants due to its structural compatibility with neurotransmitter analogs. Also utilized in agrochemical research for designing novel herbicides and plant growth regulators, leveraging the electron-withdrawing effect of fluorine to modulate compound reactivity. Its carboxylic acid functionality allows for easy derivatization into esters, amides, or peptides for structure-activity relationship (SAR) studies.
Sizes / Availability / Pricing:
Size | Availability | Price | Quantity |
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250mg | 10-20 days | ฿3,110.00 |
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1g | 10-20 days | ฿4,800.00 |
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5g | 10-20 days | ฿16,000.00 |
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25g | 10-20 days | ฿57,600.00 |
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4-Fluoro-3-methoxyphenylacetic acid
Used in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs) for central nervous system (CNS) drugs. It serves as a building block in the preparation of fluorinated analogs of bioactive molecules, where the fluorine atom enhances metabolic stability and membrane permeability. Commonly employed in the production of selective serotonin reuptake inhibitors (SSRIs) and related antidepressants due to its structural compatibility with neurotransmitter analogs. Also utilized in agrochemical research for designing novel herbicides and plant growth regulators, leveraging the electron-withdrawing effect of fluorine to modulate compound reactivity. Its carboxylic acid functionality allows for easy derivatization into esters, amides, or peptides for structure-activity relationship (SAR) studies.
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