4-Chloro-4'-fluorobutyrophenone

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Reagent Code: #158594
label
Alias 4-Chloro-4'-Fluorophenone
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CAS Number 3874-54-2

science Other reagents with same CAS 3874-54-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 200.64 g/mol
Formula C₁₀H₁₀ClFO
badge Registry Numbers
EC Number 223-395-3
MDL Number MFCD00001007
thermostat Physical Properties
Melting Point 5-6 °C
Boiling Point 130-132 °C (0.97513 mmHg)
inventory_2 Storage & Handling
Density 1.22 g/mL at 25 °C(lit.)
Storage 2~8°C

description Product Description

Used as a key intermediate in the synthesis of antipsychotic medications, such as haloperidol, and other central nervous system (CNS) agents. The compound's structure, with 4-chloro and 4'-fluoro substituted phenyl rings on a butyrophenone backbone, enables the incorporation of halogenated aromatic groups that improve metabolic stability and receptor binding in target molecules. It is widely employed in pharmaceutical research for developing neuroleptic drugs and preparing structural analogs for structure-activity relationship (SAR) studies.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿880.00
inventory 100g
10-20 days ฿3,230.00
inventory 500g
10-20 days ฿16,050.00

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4-Chloro-4'-fluorobutyrophenone
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Used as a key intermediate in the synthesis of antipsychotic medications, such as haloperidol, and other central nervous system (CNS) agents. The compound's structure, with 4-chloro and 4'-fluoro substituted phenyl rings on a butyrophenone backbone, enables the incorporation of halogenated aromatic groups that improve metabolic stability and receptor binding in target molecules. It is widely employed in pharmaceutical research for developing neuroleptic drugs and preparing structural analogs for structur

Used as a key intermediate in the synthesis of antipsychotic medications, such as haloperidol, and other central nervous system (CNS) agents. The compound's structure, with 4-chloro and 4'-fluoro substituted phenyl rings on a butyrophenone backbone, enables the incorporation of halogenated aromatic groups that improve metabolic stability and receptor binding in target molecules. It is widely employed in pharmaceutical research for developing neuroleptic drugs and preparing structural analogs for structure-activity relationship (SAR) studies.

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