6-Acetylpyridazin-3(2H)-one

95%

Reagent Code: #49575
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CAS Number 19195-01-8

science Other reagents with same CAS 19195-01-8

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Weight 138.1240 g/mol
Formula C₆H₆N₂O₂
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MDL Number MFCD24699383
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6-Acetylpyridazin-3(2H)-one is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmacologically active compounds. Its structure serves as a building block for developing molecules with potential therapeutic applications, particularly in the design of drugs targeting inflammation, cancer, and infectious diseases. Researchers leverage its reactivity to modify and optimize drug candidates, enhancing their efficacy and selectivity. Additionally, this compound is explored in agrochemical research for the development of novel pesticides and herbicides, owing to its ability to interact with biological systems in a targeted manner. Its versatility in chemical transformations makes it a valuable tool in organic synthesis for creating diverse heterocyclic compounds with industrial and scientific relevance.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,849.00

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6-Acetylpyridazin-3(2H)-one
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6-Acetylpyridazin-3(2H)-one is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmacologically active compounds. Its structure serves as a building block for developing molecules with potential therapeutic applications, particularly in the design of drugs targeting inflammation, cancer, and infectious diseases. Researchers leverage its reactivity to modify and optimize drug candidates, enhancing their efficacy and selectivity. Additionally, this

6-Acetylpyridazin-3(2H)-one is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmacologically active compounds. Its structure serves as a building block for developing molecules with potential therapeutic applications, particularly in the design of drugs targeting inflammation, cancer, and infectious diseases. Researchers leverage its reactivity to modify and optimize drug candidates, enhancing their efficacy and selectivity. Additionally, this compound is explored in agrochemical research for the development of novel pesticides and herbicides, owing to its ability to interact with biological systems in a targeted manner. Its versatility in chemical transformations makes it a valuable tool in organic synthesis for creating diverse heterocyclic compounds with industrial and scientific relevance.

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