3-(2-(Trifluoromethyl)phenyl)propiolic acid

98%

Reagent Code: #238411
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CAS Number 2806-31-7

science Other reagents with same CAS 2806-31-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.14 g/mol
Formula C₁₀H₅F₃O₂
badge Registry Numbers
MDL Number MFCD18853590
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, light-proof

description Product Description

Used in organic synthesis as a building block for pharmaceuticals and agrochemicals, particularly in the preparation of fluorinated compounds with enhanced metabolic stability and bioavailability. Its alkyne and carboxylic acid functional groups allow for participation in coupling reactions, such as Sonogashira or click chemistry, enabling the construction of complex molecular architectures. Commonly employed in the development of bioactive molecules where the trifluoromethyl group contributes to improved lipophilicity and binding affinity. Also utilized in materials science for designing specialty monomers and functional polymers with unique electronic or thermal properties.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿21,410.00
inventory 1g
10-20 days ฿57,760.00
inventory 5g
10-20 days ฿202,180.00
3-(2-(Trifluoromethyl)phenyl)propiolic acid
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Used in organic synthesis as a building block for pharmaceuticals and agrochemicals, particularly in the preparation of fluorinated compounds with enhanced metabolic stability and bioavailability. Its alkyne and carboxylic acid functional groups allow for participation in coupling reactions, such as Sonogashira or click chemistry, enabling the construction of complex molecular architectures. Commonly employed in the development of bioactive molecules where the trifluoromethyl group contributes to improve

Used in organic synthesis as a building block for pharmaceuticals and agrochemicals, particularly in the preparation of fluorinated compounds with enhanced metabolic stability and bioavailability. Its alkyne and carboxylic acid functional groups allow for participation in coupling reactions, such as Sonogashira or click chemistry, enabling the construction of complex molecular architectures. Commonly employed in the development of bioactive molecules where the trifluoromethyl group contributes to improved lipophilicity and binding affinity. Also utilized in materials science for designing specialty monomers and functional polymers with unique electronic or thermal properties.

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