6-Hydroxy-4-(trifluoromethyl)nicotinic acid

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Reagent Code: #196696
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CAS Number 849020-87-7

science Other reagents with same CAS 849020-87-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 207.109 g/mol
Formula C₇H₄F₃NO₃
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of the fungicide cyflufenamid, which is highly effective against powdery mildew in crops such as grapes, tomatoes, potatoes, and cucurbits. The trifluoromethyl and hydroxy functional groups provide enhanced metabolic stability and binding affinity in the active compounds. It is also utilized in the production of other fluorine-containing nicotinic acid derivatives for crop protection agents. Additionally, its structural similarity to nicotinic acid derivatives makes it valuable in research for designing new bioactive molecules, including potential pharmaceutical applications involving enzyme inhibition.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,640.00
inventory 1g
10-20 days ฿9,000.00
inventory 5g
10-20 days ฿27,670.00
inventory 10g
10-20 days ฿47,060.00
inventory 25g
10-20 days ฿103,430.00

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6-Hydroxy-4-(trifluoromethyl)nicotinic acid
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Used as a key intermediate in the synthesis of the fungicide cyflufenamid, which is highly effective against powdery mildew in crops such as grapes, tomatoes, potatoes, and cucurbits. The trifluoromethyl and hydroxy functional groups provide enhanced metabolic stability and binding affinity in the active compounds. It is also utilized in the production of other fluorine-containing nicotinic acid derivatives for crop protection agents. Additionally, its structural similarity to nicotinic acid derivatives

Used as a key intermediate in the synthesis of the fungicide cyflufenamid, which is highly effective against powdery mildew in crops such as grapes, tomatoes, potatoes, and cucurbits. The trifluoromethyl and hydroxy functional groups provide enhanced metabolic stability and binding affinity in the active compounds. It is also utilized in the production of other fluorine-containing nicotinic acid derivatives for crop protection agents. Additionally, its structural similarity to nicotinic acid derivatives makes it valuable in research for designing new bioactive molecules, including potential pharmaceutical applications involving enzyme inhibition.

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