4-(4-(Trifluoromethyl)phenyl)butanoic acid

95%

Reagent Code: #242839
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CAS Number 136295-01-7

science Other reagents with same CAS 136295-01-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 232.20 g/mol
Formula C₁₁H₁₁F₃O₂
badge Registry Numbers
MDL Number MFCD06810491
thermostat Physical Properties
Boiling Point 297.9±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.266±0.06 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and central nervous system agents. Its structure supports the design of compounds with enhanced metabolic stability and binding affinity due to the presence of the trifluoromethyl group. Commonly employed in medicinal chemistry for optimizing drug candidates targeting neurological disorders and chronic pain. Also utilized in the preparation of specialty organic molecules requiring fluorinated building blocks for improved pharmacokinetic properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,800.00
inventory 250mg
10-20 days ฿7,200.00
inventory 1g
10-20 days ฿14,400.00
inventory 5g
10-20 days ฿32,000.00

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4-(4-(Trifluoromethyl)phenyl)butanoic acid
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and central nervous system agents. Its structure supports the design of compounds with enhanced metabolic stability and binding affinity due to the presence of the trifluoromethyl group. Commonly employed in medicinal chemistry for optimizing drug candidates targeting neurological disorders and chronic pain. Also utilized in the preparation of specialty organic molecules requiring fluorinated

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and central nervous system agents. Its structure supports the design of compounds with enhanced metabolic stability and binding affinity due to the presence of the trifluoromethyl group. Commonly employed in medicinal chemistry for optimizing drug candidates targeting neurological disorders and chronic pain. Also utilized in the preparation of specialty organic molecules requiring fluorinated building blocks for improved pharmacokinetic properties.

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