(R)-6-(4-Aminophenyl)-5-methyl-4,5-dihydropyridazin-3(2H)-one

95%

Reagent Code: #230165
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CAS Number 101328-85-2

science Other reagents with same CAS 101328-85-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 203.24 g/mol
Formula C₁₁H₁₃N₃O
thermostat Physical Properties
Melting Point 206-208°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in the pharmaceutical industry as a key intermediate in the synthesis of antihypertensive drugs, particularly in the production of beta-adrenergic receptor blockers. Its chiral structure makes it valuable for developing enantiomerically pure medications, improving efficacy and reducing side effects. Also investigated for potential applications in central nervous system agents due to its ability to cross the blood-brain barrier. Commonly employed in research settings for structure-activity relationship studies in cardiovascular and neurological drug development.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿880.00
inventory 250mg
10-20 days ฿2,080.00
inventory 1g
10-20 days ฿4,640.00

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(R)-6-(4-Aminophenyl)-5-methyl-4,5-dihydropyridazin-3(2H)-one
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Used in the pharmaceutical industry as a key intermediate in the synthesis of antihypertensive drugs, particularly in the production of beta-adrenergic receptor blockers. Its chiral structure makes it valuable for developing enantiomerically pure medications, improving efficacy and reducing side effects. Also investigated for potential applications in central nervous system agents due to its ability to cross the blood-brain barrier. Commonly employed in research settings for structure-activity relationsh

Used in the pharmaceutical industry as a key intermediate in the synthesis of antihypertensive drugs, particularly in the production of beta-adrenergic receptor blockers. Its chiral structure makes it valuable for developing enantiomerically pure medications, improving efficacy and reducing side effects. Also investigated for potential applications in central nervous system agents due to its ability to cross the blood-brain barrier. Commonly employed in research settings for structure-activity relationship studies in cardiovascular and neurological drug development.

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