4-amino-2,4-dihydro-1H-isoquinolin-3-one


Chemical Name: 4-amino-2,4-dihydro-1H-isoquinolin-3-one
CAS Number: 209983-18-6
Product Number: AG002KHG(AGN-PC-03NTPY)
Synonyms:
MDL No:
Molecular Formula: C9H10N2O
Molecular Weight: 162.1885

Identification/Properties


Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319
Precautionary Statements:
P264-P280-P302+P352-P305+P351+P338-P321-P332+P313-P337+P313-P362
Class:
-
Packing Group:
-

NMR Spectrum


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Chemical Structure



4-Amino-1,2-dihydroisoquinolin-3(4H)-one, commonly known as $name$, is a versatile compound widely used in chemical synthesis applications. Due to its unique structure and reactivity, $name$ serves as a crucial building block in the creation of various organic compounds. In the realm of synthetic chemistry, $name$ is particularly valued for its role in the synthesis of pharmaceuticals, dyes, and complex organic molecules.One significant application of $name$ in chemical synthesis is its incorporation into the synthesis of heterocyclic compounds. By utilizing $name$ as a starting material, chemists can access a diverse range of heterocycles, enabling the production of biologically active molecules and materials with specific properties. The presence of the amino and carbonyl groups in $name$ facilitates its involvement in numerous synthetic pathways, allowing for the efficient construction of complex structures.Furthermore, the reactivity of $name$ makes it an ideal candidate for functionalization reactions. Chemists can modify the amino group or the carbonyl group of $name$ to introduce various functional groups, thus expanding the compound's synthetic utility. This versatility in functionalization enables tailored modifications to suit specific synthetic goals and target applications. Overall, the unique structural features and reactivity of $name$ make it a valuable tool in the toolkit of organic chemists seeking to access diverse chemical space and develop innovative synthetic routes.