N-benzyl-2-chloro-8-methoxyquinazolin-4-amine

95%

Reagent Code: #219087
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CAS Number 124309-70-2

science Other reagents with same CAS 124309-70-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 299.75 g/mol
Formula C₁₆H₁₄ClN₃O
badge Registry Numbers
MDL Number MFCD30721684
thermostat Physical Properties
Boiling Point 441.2±27.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.325±0.06 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to enzyme active sites, making it valuable in designing drugs that target tyrosine kinase pathways. Commonly employed in medicinal chemistry research to optimize potency and selectivity in antitumor compounds. Also utilized in the preparation of bioactive molecules for studying cell signaling mechanisms. Additionally, it serves as an intermediate for synthesizing quinazoline derivatives with other biological activities, such as antimicrobial and anti-inflammatory effects. Currently, it is primarily used in laboratory research and not widely applied in clinical settings.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿19,960.00
250mg
10-20 days ฿31,970.00
1g
10-20 days ฿80,020.00
N-benzyl-2-chloro-8-methoxyquinazolin-4-amine
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to enzyme active sites, making it valuable in designing drugs that target tyrosine kinase pathways. Commonly employed in medicinal chemistry research to optimize potency and selectivity in antitumor compounds. Also utilized in the preparation of bioactive molecules for studying cell signaling mechanisms. Additionally, it serves as

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to enzyme active sites, making it valuable in designing drugs that target tyrosine kinase pathways. Commonly employed in medicinal chemistry research to optimize potency and selectivity in antitumor compounds. Also utilized in the preparation of bioactive molecules for studying cell signaling mechanisms. Additionally, it serves as an intermediate for synthesizing quinazoline derivatives with other biological activities, such as antimicrobial and anti-inflammatory effects. Currently, it is primarily used in laboratory research and not widely applied in clinical settings.

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