7-chloro-2-methylquinazolin-4(3H)-one

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Reagent Code: #196827
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CAS Number 7012-88-6

science Other reagents with same CAS 7012-88-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 194.62 g/mol
Formula C₉H₇ClN₂O
badge Registry Numbers
MDL Number MFCD11048436
thermostat Physical Properties
Melting Point 262-263 °C
Boiling Point 333.6°C at 760 mmHg
inventory_2 Storage & Handling
Density 1.43 g/cm3
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical agents, particularly in the development of antihypertensive and anti-inflammatory drugs. It serves as a building block for quinazoline-based compounds that exhibit kinase inhibition activity, making it valuable in research for anticancer agents. Also employed in the preparation of derivatives for studying structure-activity relationships in central nervous system depressants. Its scaffold is explored in medicinal chemistry for optimizing drug candidates with improved metabolic stability and binding affinity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,740.00
inventory 250mg
10-20 days ฿6,790.00
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7-chloro-2-methylquinazolin-4(3H)-one
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Used as an intermediate in the synthesis of pharmaceutical agents, particularly in the development of antihypertensive and anti-inflammatory drugs. It serves as a building block for quinazoline-based compounds that exhibit kinase inhibition activity, making it valuable in research for anticancer agents. Also employed in the preparation of derivatives for studying structure-activity relationships in central nervous system depressants. Its scaffold is explored in medicinal chemistry for optimizing drug can

Used as an intermediate in the synthesis of pharmaceutical agents, particularly in the development of antihypertensive and anti-inflammatory drugs. It serves as a building block for quinazoline-based compounds that exhibit kinase inhibition activity, making it valuable in research for anticancer agents. Also employed in the preparation of derivatives for studying structure-activity relationships in central nervous system depressants. Its scaffold is explored in medicinal chemistry for optimizing drug candidates with improved metabolic stability and binding affinity.

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