6-Chloro-3-(4-fluorophenyl)picolinic acid

95%

Reagent Code: #162293
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CAS Number 1214381-04-0

science Other reagents with same CAS 1214381-04-0

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Weight 251.64 g/mol
Formula C₁₂H₇ClFNO₂
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MDL Number MFCD14700774
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its halogenated aromatic structure, which enhances binding selectivity and metabolic stability in drug candidates. Also employed in the preparation of agrochemicals and bioactive molecules where fluorinated and chlorinated heterocycles improve efficacy and environmental persistence. Its carboxylic acid functionality allows for easy derivatization into amides, esters, and other functional groups critical in structure-activity relationship studies.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿19,200.00
inventory 100mg
10-20 days ฿51,200.00

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6-Chloro-3-(4-fluorophenyl)picolinic acid
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its halogenated aromatic structure, which enhances binding selectivity and metabolic stability in drug candidates. Also employed in the preparation of agrochemicals and bioactive molecules where fluorinated and chlorinated heterocycles improve efficacy and environmental persistence. Its carboxylic acid

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its halogenated aromatic structure, which enhances binding selectivity and metabolic stability in drug candidates. Also employed in the preparation of agrochemicals and bioactive molecules where fluorinated and chlorinated heterocycles improve efficacy and environmental persistence. Its carboxylic acid functionality allows for easy derivatization into amides, esters, and other functional groups critical in structure-activity relationship studies.

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