6-Hydroxy-2-(trifluoromethyl)nicotinic acid

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Reagent Code: #197084
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CAS Number 862111-58-8

science Other reagents with same CAS 862111-58-8

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Weight 207.11 g/mol
Formula C₇H₄F₃NO₃
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and plant growth regulators. Its trifluoromethyl and hydroxy functional groups enhance binding selectivity and metabolic stability in active compounds. Commonly employed in the production of fluorine-containing nicotinic acid derivatives, which show improved biological activity and environmental persistence. Also utilized in research for designing novel bioactive molecules due to its structural similarity to natural nicotinic acids.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,900.00
inventory 250mg
10-20 days ฿14,190.00
inventory 1g
10-20 days ฿36,880.00
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6-Hydroxy-2-(trifluoromethyl)nicotinic acid
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Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and plant growth regulators. Its trifluoromethyl and hydroxy functional groups enhance binding selectivity and metabolic stability in active compounds. Commonly employed in the production of fluorine-containing nicotinic acid derivatives, which show improved biological activity and environmental persistence. Also utilized in research for designing novel bioactive molecules due t

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and plant growth regulators. Its trifluoromethyl and hydroxy functional groups enhance binding selectivity and metabolic stability in active compounds. Commonly employed in the production of fluorine-containing nicotinic acid derivatives, which show improved biological activity and environmental persistence. Also utilized in research for designing novel bioactive molecules due to its structural similarity to natural nicotinic acids.

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