logo
Home  > 4-(4-Aminophenoxy)pyridin-2(1h)-one

AE24884

1041861-94-2 | 4-(4-Aminophenoxy)pyridin-2(1h)-one

Packsize Purity Availability Price Discounted Price    Quantity
100mg 95% in stock $128.00 $90.00 -   +
250mg 95% in stock $178.00 $125.00 -   +
1g 95% in stock $458.00 $321.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AE24884
Chemical Name: 4-(4-Aminophenoxy)pyridin-2(1h)-one
CAS Number: 1041861-94-2
Molecular Formula: C11H10N2O2
Molecular Weight: 202.2093
MDL Number: MFCD24038953
SMILES: Nc1ccc(cc1)Oc1cc[nH]c(=O)c1

 

Upstream Synthesis Route
  • 4-(4-Aminophenoxy)pyridin-2(1H)-one, also known as $name$, is a versatile compound that finds wide application in chemical synthesis. Known for its unique structure and reactivity, this compound plays a crucial role in the creation of various organic molecules through synthetic pathways.In chemical synthesis, 4-(4-Aminophenoxy)pyridin-2(1H)-one serves as a key building block in the preparation of novel pharmaceuticals, agrochemicals, and other specialty chemicals. Its distinctive aromatic ring system, along with the presence of an amino group and a carbonyl group, enables it to participate in a range of important reactions, such as nucleophilic substitution, oxidative coupling, and transition metal-catalyzed transformations.The amino group in 4-(4-Aminophenoxy)pyridin-2(1H)-one can act as a nucleophile, allowing for the introduction of various functional groups to tailor the compound for specific applications. Additionally, the pyridine ring confers unique reactivity patterns, making it a valuable component in the design and synthesis of complex organic molecules.Overall, the versatility and reactivity of 4-(4-Aminophenoxy)-pyridin-2(1H)-one make it an indispensable tool for chemists and researchers engaged in the development of new materials and biologically active compounds. Its role in chemical synthesis underscores its importance as a valuable building block in the creation of diverse molecular architectures.
FEATURED PRODUCTS