(S)-2-(2-Fluoro-[1,1'-biphenyl]-4-yl)propanoic acid

98%

Reagent Code: #236409
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CAS Number 51543-39-6

science Other reagents with same CAS 51543-39-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 244.26 g/mol
Formula C₁₅H₁₃FO₂
badge Registry Numbers
MDL Number MFCD00866152
thermostat Physical Properties
Melting Point 109-110 °C
Boiling Point 376.2 °C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a chiral intermediate in the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs), particularly in the production of active enantiomers with enhanced pharmacological activity. Its structure allows for selective binding to cyclooxygenase enzymes, contributing to reduced inflammation and pain. Commonly employed in asymmetric synthesis routes where stereochemistry plays a critical role in drug efficacy. Also utilized in the development of novel biphenyl-based pharmaceuticals due to its metabolic stability and favorable bioavailability profile.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿19,800.00
inventory 1g
10-20 days ฿74,150.00
inventory 100mg
10-20 days ฿11,140.00
(S)-2-(2-Fluoro-[1,1'-biphenyl]-4-yl)propanoic acid
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Used as a chiral intermediate in the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs), particularly in the production of active enantiomers with enhanced pharmacological activity. Its structure allows for selective binding to cyclooxygenase enzymes, contributing to reduced inflammation and pain. Commonly employed in asymmetric synthesis routes where stereochemistry plays a critical role in drug efficacy. Also utilized in the development of novel biphenyl-based pharmaceuticals due to its metabo

Used as a chiral intermediate in the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs), particularly in the production of active enantiomers with enhanced pharmacological activity. Its structure allows for selective binding to cyclooxygenase enzymes, contributing to reduced inflammation and pain. Commonly employed in asymmetric synthesis routes where stereochemistry plays a critical role in drug efficacy. Also utilized in the development of novel biphenyl-based pharmaceuticals due to its metabolic stability and favorable bioavailability profile.

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