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Catalog Number:
29369
CAS Number:
216099-46-6
6-Aminoisoquinolin-1(2 H -ona
Purity:
≥ 97 % (HPLC)
Synonym(s):
6-amino-1,2-dihidroisoquinolin-1-ona
Documents
$168.35 /100 mg
Tamaño
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Product Information

6-Aminoisoquinolin-1(2H)-one is a versatile compound recognized for its significant role in pharmaceutical research and development. This heterocyclic compound features an amino group that enhances its reactivity and potential as a building block in the synthesis of various bioactive molecules. Its unique structure allows for applications in medicinal chemistry, particularly in the development of novel therapeutic agents targeting neurological disorders and cancer. Researchers have found that derivatives of 6-Aminoisoquinolin-1(2H)-one exhibit promising biological activities, making it a valuable candidate for further exploration in drug discovery.

In addition to its pharmaceutical applications, 6-Aminoisoquinolin-1(2H)-one can also serve as an important intermediate in organic synthesis, facilitating the creation of complex molecular architectures. Its ability to participate in various chemical reactions, such as coupling and cyclization, underscores its utility in developing new materials and compounds. With its favorable properties and potential for innovation, 6-Aminoisoquinolin-1(2H)-one stands out as a compound of interest for researchers and industry professionals seeking to advance their projects in drug development and synthetic chemistry.

Synonyms
6-amino-1,2-dihidroisoquinolin-1-ona
CAS Number
216099-46-6
Purity
≥ 97 % (HPLC)
Molecular Formula
C9H8N2O
Molecular Weight
160.18
MDL Number
MFCD12547311
PubChem ID
51342001
Appearance
Sólido de color amarillo claro o pálido
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
6-amino-1,2-dihidroisoquinolin-1-ona
CAS Number
216099-46-6
Purity
≥ 97 % (HPLC)
Molecular Formula
C9H8N2O
Molecular Weight
160.18
MDL Number
MFCD12547311
PubChem ID
51342001
Appearance
Sólido de color amarillo claro o pálido
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

6-Aminoisoquinolin-1(2H)-one is widely utilized in research focused on

  • Pharmaceutical Development: This compound serves as a key intermediate in synthesizing various pharmaceuticals, particularly in the development of drugs targeting neurological disorders.
  • Biological Research: It is used in studies investigating its effects on cellular processes, helping researchers understand its potential as a therapeutic agent.
  • Chemical Synthesis: The compound acts as a building block in organic synthesis, allowing chemists to create more complex molecules efficiently.
  • Fluorescent Probes: It can be incorporated into fluorescent probes for imaging applications, enhancing the visualization of biological samples under a microscope.
  • Material Science: This chemical is explored for its potential in developing new materials, particularly in creating polymers with unique properties.

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