4-Chloro-1-(4-hydroxyphenyl)butan-1-one

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Reagent Code: #160407
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CAS Number 7150-55-2

science Other reagents with same CAS 7150-55-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 198.65 g/mol
Formula C₁₀H₁₁ClO₂
thermostat Physical Properties
Melting Point 105-10°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in the synthesis of central nervous system (CNS) pharmaceuticals, particularly antipsychotics and other neuroactive agents. It serves as a building block for compounds targeting neurotransmitter modulation, such as dopamine antagonists for treating psychiatric disorders. The phenolic hydroxyl and carbonyl groups enable versatile modifications in organic synthesis, while the 4-chlorobutyl chain facilitates nucleophilic substitutions to incorporate heterocyclic rings. Valuable in medicinal chemistry for developing new CNS drug candidates and exploring structure-activity relationships.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,390.00
inventory 1g
10-20 days ฿4,890.00
inventory 5g
10-20 days ฿17,160.00

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4-Chloro-1-(4-hydroxyphenyl)butan-1-one
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Used as an intermediate in the synthesis of central nervous system (CNS) pharmaceuticals, particularly antipsychotics and other neuroactive agents. It serves as a building block for compounds targeting neurotransmitter modulation, such as dopamine antagonists for treating psychiatric disorders. The phenolic hydroxyl and carbonyl groups enable versatile modifications in organic synthesis, while the 4-chlorobutyl chain facilitates nucleophilic substitutions to incorporate heterocyclic rings. Valuable in medic
Used as an intermediate in the synthesis of central nervous system (CNS) pharmaceuticals, particularly antipsychotics and other neuroactive agents. It serves as a building block for compounds targeting neurotransmitter modulation, such as dopamine antagonists for treating psychiatric disorders. The phenolic hydroxyl and carbonyl groups enable versatile modifications in organic synthesis, while the 4-chlorobutyl chain facilitates nucleophilic substitutions to incorporate heterocyclic rings. Valuable in medicinal chemistry for developing new CNS drug candidates and exploring structure-activity relationships.
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