2-(Chloromethyl)-4-methylquinazoline

98%

Reagent Code: #159115
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CAS Number 109113-72-6

science Other reagents with same CAS 109113-72-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 192.64 g/mol
Formula C₁₀H₉ClN₂
badge Registry Numbers
MDL Number MFCD09807547
inventory_2 Storage & Handling
Density 1.251 g/cm3
Storage Room temperature

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antihypertensive agents and alpha-adrenergic blockers. It serves as a key building block in the preparation of quinazoline-based drugs, which are known for their activity in cardiovascular and central nervous system therapies. Its reactive chloromethyl group allows for easy alkylation or coupling with other moieties, making it valuable in medicinal chemistry for constructing complex drug molecules. Also employed in research settings to develop new bioactive compounds and in the creation of libraries for high-throughput screening in drug discovery.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿168.00
inventory 25g
10-20 days ฿1,490.00
inventory 100g
10-20 days ฿5,900.00
inventory 5g
10-20 days ฿360.00
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2-(Chloromethyl)-4-methylquinazoline
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Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antihypertensive agents and alpha-adrenergic blockers. It serves as a key building block in the preparation of quinazoline-based drugs, which are known for their activity in cardiovascular and central nervous system therapies. Its reactive chloromethyl group allows for easy alkylation or coupling with other moieties, making it valuable in medicinal chemistry for constructing complex drug molecules. A

Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antihypertensive agents and alpha-adrenergic blockers. It serves as a key building block in the preparation of quinazoline-based drugs, which are known for their activity in cardiovascular and central nervous system therapies. Its reactive chloromethyl group allows for easy alkylation or coupling with other moieties, making it valuable in medicinal chemistry for constructing complex drug molecules. Also employed in research settings to develop new bioactive compounds and in the creation of libraries for high-throughput screening in drug discovery.

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