1(2H)-Isoquinolinone, 7-hydroxy-|59647-24-4,AngeneChemical

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1(2H)-Isoquinolinone, 7-hydroxy-

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Chemical Name:	1(2H)-Isoquinolinone, 7-hydroxy-
CAS Number:	59647-24-4
Product Number:	AG00F2A1(AGN-PC-00KGEY)
Synonyms:
MDL No:
Molecular Formula:	C9H7NO2
Molecular Weight:	161.1574

Identification/Properties
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NMR Spectrum
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Identification/Properties

Computed Properties

Molecular Weight:

161.16g/mol

XLogP3:

Hydrogen Bond Donor Count:

Hydrogen Bond Acceptor Count:

Rotatable Bond Count:

Exact Mass:

161.048g/mol

Monoisotopic Mass:

161.048g/mol

Topological Polar Surface Area:

49.3A^2

Heavy Atom Count:

Formal Charge:

Complexity:

225

Isotope Atom Count:

Defined Atom Stereocenter Count:

Undefined Atom Stereocenter Count:

Defined Bond Stereocenter Count:

Undefined Bond Stereocenter Count:

Covalently-Bonded Unit Count:

Compound Is Canonicalized:

Yes

Safety Information

GHS Pictogram:

N/A

Signal Word:

UN#:

Hazard Statements:

Precautionary Statements:

Class:

Packing Group:

NMR Spectrum

Other Analytical Data

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Chemical Structure

7-Hydroxyisoquinolin-1(2H)-one is a versatile compound widely used in chemical synthesis as a key building block for the preparation of various pharmaceuticals, agrochemicals, and other fine chemicals. Its unique structure and reactivity make it an essential component in the production of a wide range of important organic compounds.In chemical synthesis, 7-Hydroxyisoquinolin-1(2H)-one serves as a valuable intermediate for the synthesis of biologically active molecules such as antiviral agents, anticancer drugs, and enzyme inhibitors. Its ability to undergo various functional group transformations, such as alkylation, acylation, and condensation reactions, enables chemists to introduce specific functional groups at desired positions in the molecule, leading to the creation of novel and diverse chemical entities.Furthermore, 7-Hydroxyisoquinolin-1(2H)-one can be utilized in the development of efficient synthetic routes for the production of complex molecules with high structural diversity. Its presence in the synthesis of natural products and heterocyclic compounds highlights its importance as a valuable scaffold for designing new compounds with potential therapeutic applications.Overall, the application of 7-Hydroxyisoquinolin-1(2H)-one in chemical synthesis plays a crucial role in the discovery and development of novel pharmaceuticals and other bioactive compounds, demonstrating its significance in modern organic chemistry research and drug discovery efforts.