5-Amino-2-methyl-2,3-dihydropyridazin-3-one

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Reagent Code: #139433
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CAS Number 13506-27-9

science Other reagents with same CAS 13506-27-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 125.13 g/mol
Formula C₅H₇N₃O
badge Registry Numbers
MDL Number MFCD19204146
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of cardiovascular drugs and antihypertensive agents. It serves as a building block for pyridazine-containing compounds which exhibit biological activity, including vasodilatory and positive inotropic effects. Also employed in research for the preparation of novel heterocyclic compounds with potential therapeutic applications. Its reactivity allows for functionalization at the amino and carbonyl groups, enabling diverse chemical modifications for drug discovery and optimization.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿17,470.00
250mg
10-20 days ฿27,920.00
500mg
10-20 days ฿46,490.00
1g
10-20 days ฿69,800.00

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5-Amino-2-methyl-2,3-dihydropyridazin-3-one
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of cardiovascular drugs and antihypertensive agents. It serves as a building block for pyridazine-containing compounds which exhibit biological activity, including vasodilatory and positive inotropic effects. Also employed in research for the preparation of novel heterocyclic compounds with potential therapeutic applications. Its reactivity allows for functionalization at the amino and carbonyl groups, enabling d

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of cardiovascular drugs and antihypertensive agents. It serves as a building block for pyridazine-containing compounds which exhibit biological activity, including vasodilatory and positive inotropic effects. Also employed in research for the preparation of novel heterocyclic compounds with potential therapeutic applications. Its reactivity allows for functionalization at the amino and carbonyl groups, enabling diverse chemical modifications for drug discovery and optimization.

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