3'-Chloro-4'-fluoro-[1,1'-biphenyl]-2-amine

97%

Reagent Code: #166546
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CAS Number 577954-86-0

science Other reagents with same CAS 577954-86-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 221.66 g/mol
Formula C₁₂H₉ClFN
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of non-steroidal anti-inflammatory drugs (NSAIDs) and selective COX-2 inhibitors. Its structure allows for effective modulation of biological activity in drug candidates targeting inflammation and pain. Commonly employed in medicinal chemistry for constructing biaryl scaffolds with enhanced metabolic stability and target binding affinity. Also utilized in agrochemical research for designing novel herbicides and fungicides due to its halogenated aromatic framework that improves lipophilicity and bioavailability.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,530.00
inventory 250mg
10-20 days ฿11,060.00
inventory 1g
10-20 days ฿27,660.00
inventory 5g
10-20 days ฿58,240.00

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3'-Chloro-4'-fluoro-[1,1'-biphenyl]-2-amine
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of non-steroidal anti-inflammatory drugs (NSAIDs) and selective COX-2 inhibitors. Its structure allows for effective modulation of biological activity in drug candidates targeting inflammation and pain. Commonly employed in medicinal chemistry for constructing biaryl scaffolds with enhanced metabolic stability and target binding affinity. Also utilized in agrochemical research for designing novel herbici

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of non-steroidal anti-inflammatory drugs (NSAIDs) and selective COX-2 inhibitors. Its structure allows for effective modulation of biological activity in drug candidates targeting inflammation and pain. Commonly employed in medicinal chemistry for constructing biaryl scaffolds with enhanced metabolic stability and target binding affinity. Also utilized in agrochemical research for designing novel herbicides and fungicides due to its halogenated aromatic framework that improves lipophilicity and bioavailability.

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