4-(4-Chlorobenzyl)-2H-phthalazin-1-one

98%

Reagent Code: #159885
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CAS Number 53242-88-9

science Other reagents with same CAS 53242-88-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 270.71 g/mol
Formula C₁₅H₁₁ClN₂O
badge Registry Numbers
MDL Number MFCD02168779
thermostat Physical Properties
Boiling Point 522.3 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.32 g/cm3
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment and phosphodiesterase (PDE) inhibitors for central nervous system (CNS) disorders such as depression and sleep aids. It serves as a versatile building block in medicinal chemistry due to its ability to interact with biological targets through hydrogen bonding and hydrophobic interactions. Its structure is often modified to enhance potency, selectivity, and reduce side effects in drug candidates. Also employed in research settings for structure-activity relationship (SAR) studies, as well as in the development of anti-inflammatory agents.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,570.00
inventory 1g
10-20 days ฿11,430.00

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4-(4-Chlorobenzyl)-2H-phthalazin-1-one
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment and phosphodiesterase (PDE) inhibitors for central nervous system (CNS) disorders such as depression and sleep aids. It serves as a versatile building block in medicinal chemistry due to its ability to interact with biological targets through hydrogen bonding and hydrophobic interactions. Its structure is often modified to enhance potency, selectivity, and reduce

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment and phosphodiesterase (PDE) inhibitors for central nervous system (CNS) disorders such as depression and sleep aids. It serves as a versatile building block in medicinal chemistry due to its ability to interact with biological targets through hydrogen bonding and hydrophobic interactions. Its structure is often modified to enhance potency, selectivity, and reduce side effects in drug candidates. Also employed in research settings for structure-activity relationship (SAR) studies, as well as in the development of anti-inflammatory agents.

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