4,5-DIHYDRO-6-PHENYL-3(2H)-PYRIDAZINONE

98 %

Reagent Code: #170585
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CAS Number 1011-46-7

science Other reagents with same CAS 1011-46-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 174.20 g/mol
Formula C₁₀H₁₀N₂O
badge Registry Numbers
MDL Number MFCD00099597
thermostat Physical Properties
Melting Point 151-154°C (Lit.)
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and biologically active compounds. Shows potential in the development of cardiovascular drugs due to its structural similarity to known vasodilators. Also investigated for its role in the preparation of pyridazine-based heterocycles, which are important in medicinal chemistry for their enzyme inhibitory properties. Employed in research settings to explore new pathways for nitrogen-containing ring systems with possible antihypertensive and anti-inflammatory effects.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,260.00
inventory 1g
10-20 days ฿7,240.00

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4,5-DIHYDRO-6-PHENYL-3(2H)-PYRIDAZINONE
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Used in organic synthesis as an intermediate for pharmaceuticals and biologically active compounds. Shows potential in the development of cardiovascular drugs due to its structural similarity to known vasodilators. Also investigated for its role in the preparation of pyridazine-based heterocycles, which are important in medicinal chemistry for their enzyme inhibitory properties. Employed in research settings to explore new pathways for nitrogen-containing ring systems with possible antihypertensive and a

Used in organic synthesis as an intermediate for pharmaceuticals and biologically active compounds. Shows potential in the development of cardiovascular drugs due to its structural similarity to known vasodilators. Also investigated for its role in the preparation of pyridazine-based heterocycles, which are important in medicinal chemistry for their enzyme inhibitory properties. Employed in research settings to explore new pathways for nitrogen-containing ring systems with possible antihypertensive and anti-inflammatory effects.

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