4(3H)-Quinazolinone, 2-[[4-[2-(4-chlorophenoxy)acetyl]-1-piperazinyl]methyl]-3-[4-(1-methylethoxy)[1,1'-biphenyl]-3-yl]-

99%

Reagent Code: #196167
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CAS Number 1695533-44-8

science Other reagents with same CAS 1695533-44-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 623.2 g/mol
Formula C₃₆H₃₅ClN₄O₄
inventory_2 Storage & Handling
Storage 2-8°C, dry, closed

description Product Description

Used primarily as a key intermediate in the synthesis of potent angiotensin II receptor antagonists, this compound plays a critical role in developing medications for hypertension and cardiovascular diseases. Its structure enables strong binding to specific receptors, helping regulate blood pressure. Due to its lipophilic nature and stability, it enhances bioavailability in oral drug formulations. It is also explored in research for improving metabolic stability and selectivity in new antihypertensive agents.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿13,050.00
inventory 100mg
10-20 days ฿88,200.00
inventory 500mg
10-20 days ฿259,200.00
inventory 25mg
10-20 days ฿36,000.00

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4(3H)-Quinazolinone, 2-[[4-[2-(4-chlorophenoxy)acetyl]-1-piperazinyl]methyl]-3-[4-(1-methylethoxy)[1,1'-biphenyl]-3-yl]-
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Used primarily as a key intermediate in the synthesis of potent angiotensin II receptor antagonists, this compound plays a critical role in developing medications for hypertension and cardiovascular diseases. Its structure enables strong binding to specific receptors, helping regulate blood pressure. Due to its lipophilic nature and stability, it enhances bioavailability in oral drug formulations. It is also explored in research for improving metabolic stability and selectivity in new antihypertensive ag

Used primarily as a key intermediate in the synthesis of potent angiotensin II receptor antagonists, this compound plays a critical role in developing medications for hypertension and cardiovascular diseases. Its structure enables strong binding to specific receptors, helping regulate blood pressure. Due to its lipophilic nature and stability, it enhances bioavailability in oral drug formulations. It is also explored in research for improving metabolic stability and selectivity in new antihypertensive agents.

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