N-(3-Chloro-4-fluorophenyl)-7-methoxy-6-(3-(piperazin-1-yl)propoxy)quinazolin-4-amine

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Reagent Code: #51878
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CAS Number 295330-45-9

science Other reagents with same CAS 295330-45-9

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Weight 445.9176 g/mol
Formula C₂₂H₂₅ClFN₅O₂
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description Product Description

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of targeted cancer therapies. It is particularly significant in the development of tyrosine kinase inhibitors, which are designed to disrupt signaling pathways in cancer cells. The structural features of the molecule, including the quinazoline core and the piperazine moiety, enable it to effectively bind to specific kinase proteins, making it a valuable component in the creation of drugs for treating cancers such as non-small cell lung cancer and breast cancer. Additionally, its modified aromatic and heterocyclic components contribute to enhanced bioavailability and selectivity, optimizing its therapeutic potential.

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inventory 100mg
10-20 days ฿10,530.00

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N-(3-Chloro-4-fluorophenyl)-7-methoxy-6-(3-(piperazin-1-yl)propoxy)quinazolin-4-amine
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This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of targeted cancer therapies. It is particularly significant in the development of tyrosine kinase inhibitors, which are designed to disrupt signaling pathways in cancer cells. The structural features of the molecule, including the quinazoline core and the piperazine moiety, enable it to effectively bind to specific kinase proteins, making it a valuable component in the creation of drugs for tre

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of targeted cancer therapies. It is particularly significant in the development of tyrosine kinase inhibitors, which are designed to disrupt signaling pathways in cancer cells. The structural features of the molecule, including the quinazoline core and the piperazine moiety, enable it to effectively bind to specific kinase proteins, making it a valuable component in the creation of drugs for treating cancers such as non-small cell lung cancer and breast cancer. Additionally, its modified aromatic and heterocyclic components contribute to enhanced bioavailability and selectivity, optimizing its therapeutic potential.

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