5,6-Difluoro-1H-indole-3-carboxylicacid

98%

Reagent Code: #179940
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CAS Number 959238-71-2

science Other reagents with same CAS 959238-71-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 197.14 g/mol
Formula C₉H₅F₂NO₂
badge Registry Numbers
MDL Number MFCD09954942
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system agents. Its fluorinated indole structure enhances binding affinity and metabolic stability in drug candidates. Also employed in the preparation of kinase inhibitors and anti-inflammatory agents due to its ability to modulate biological pathways. The carboxylic acid group allows for easy derivatization, making it valuable in medicinal chemistry for creating amide and ester analogs during structure-activity relationship studies.

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inventory 100mg
10-20 days ฿7,760.00

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5,6-Difluoro-1H-indole-3-carboxylicacid
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system agents. Its fluorinated indole structure enhances binding affinity and metabolic stability in drug candidates. Also employed in the preparation of kinase inhibitors and anti-inflammatory agents due to its ability to modulate biological pathways. The carboxylic acid group allows for easy derivatization, making it valuab

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system agents. Its fluorinated indole structure enhances binding affinity and metabolic stability in drug candidates. Also employed in the preparation of kinase inhibitors and anti-inflammatory agents due to its ability to modulate biological pathways. The carboxylic acid group allows for easy derivatization, making it valuable in medicinal chemistry for creating amide and ester analogs during structure-activity relationship studies.

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