5-Bromo-2-(trifluoromethyl)nicotinic acid

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Reagent Code: #153349
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CAS Number 436799-36-9

science Other reagents with same CAS 436799-36-9

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scatter_plot Molecular Information
Weight 270.0034 g/mol
Formula C₇H₃BrF₃NO₂
badge Registry Numbers
MDL Number MFCD08741350
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and bioactive molecules. Its structure supports the creation of compounds with insecticidal and herbicidal properties. Commonly employed in medicinal chemistry for constructing nitrogen-containing heterocycles, it plays a role in optimizing drug candidates targeting central nervous system disorders and inflammation. The bromo and trifluoromethyl groups allow for further functionalization via cross-coupling reactions, making it valuable in building complex molecules during drug discovery.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,740.00
inventory 250mg
10-20 days ฿10,760.00

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5-Bromo-2-(trifluoromethyl)nicotinic acid
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and bioactive molecules. Its structure supports the creation of compounds with insecticidal and herbicidal properties. Commonly employed in medicinal chemistry for constructing nitrogen-containing heterocycles, it plays a role in optimizing drug candidates targeting central nervous system disorders and inflammation. The bromo and trifluoromethyl groups allow for further functionalization via c

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and bioactive molecules. Its structure supports the creation of compounds with insecticidal and herbicidal properties. Commonly employed in medicinal chemistry for constructing nitrogen-containing heterocycles, it plays a role in optimizing drug candidates targeting central nervous system disorders and inflammation. The bromo and trifluoromethyl groups allow for further functionalization via cross-coupling reactions, making it valuable in building complex molecules during drug discovery.

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