2,4-Dichloro-7-methylquinazoline

97%

Reagent Code: #171124
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CAS Number 25171-19-1

science Other reagents with same CAS 25171-19-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 213.06 g/mol
Formula C₉H₆Cl₂N₂
thermostat Physical Properties
Melting Point 107°C
Boiling Point 292.4±33.0°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 undergo nucleophilic substitution at the 4-position, allowing for the introduction of various functional groups. Commonly employed in medicinal chemistry for structure-activity relationship studies in drug discovery programs targeting tyrosine kinase receptors. Also utilized in the production of agrochemicals and dyes where a halogenated quinazoline scaffold enhances reactivity or binding properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,180.00
inventory 250mg
10-20 days ฿7,480.00
inventory 1g
10-20 days ฿17,600.00
inventory 5g
10-20 days ฿47,250.00

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2,4-Dichloro-7-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 undergo nucleophilic substitution at the 4-position, allowing for the introduction of various functional groups. Commonly employed in medicinal chemistry for structure-activity relationship studies in drug discovery programs targeting tyrosine kinase receptors. Also utilized in

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 undergo nucleophilic substitution at the 4-position, allowing for the introduction of various functional groups. Commonly employed in medicinal chemistry for structure-activity relationship studies in drug discovery programs targeting tyrosine kinase receptors. Also utilized in the production of agrochemicals and dyes where a halogenated quinazoline scaffold enhances reactivity or binding properties.

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