4-Chloro-2-methylquinazoline

95%

Reagent Code: #160028
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CAS Number 6484-24-8

science Other reagents with same CAS 6484-24-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 178.62 g/mol
Formula C₉H₇ClN₂
thermostat Physical Properties
Melting Point 86°C
Boiling Point 211.2°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in the preparation of bioactive molecules due to its ability to engage in substitution reactions at the 4-chloro position. Commonly employed in medicinal chemistry for structure-activity relationship studies in quinazoline-based drug candidates. Also utilized in the production of agrochemicals and dyes where heterocyclic frameworks enhance stability and reactivity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿209.00
inventory 1g
10-20 days ฿1,380.00
inventory 5g
10-20 days ฿3,550.00
inventory 10g
10-20 days ฿5,730.00
inventory 25g
10-20 days ฿14,150.00

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4-Chloro-2-methylquinazoline
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in the preparation of bioactive molecules due to its ability to engage in substitution reactions at the 4-chloro position. Commonly employed in medicinal chemistry for structure-activity relationship studies in quinazoline-based drug candidates. Also utilized in the production of agrochemicals and dyes where heterocyclic frameworks enhance s

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in the preparation of bioactive molecules due to its ability to engage in substitution reactions at the 4-chloro position. Commonly employed in medicinal chemistry for structure-activity relationship studies in quinazoline-based drug candidates. Also utilized in the production of agrochemicals and dyes where heterocyclic frameworks enhance stability and reactivity.

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