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Catalog Number:
19286
CAS Number:
259221-99-3
Acridine-9-carboxylic acid (6-amino-hexyl)amide
Synonym(s):
N-(6-Aminohexyl)acridine-9-carboxamide
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Product Information

Acridine-9-carboxylic acid (6-amino-hexyl)amide is a versatile compound known for its unique structural properties and potential applications in various fields. This compound features an acridine backbone, which is recognized for its fluorescent properties, making it valuable in the development of fluorescent probes and dyes. Its amide functionality enhances solubility and reactivity, allowing for easy incorporation into complex molecular structures. Researchers in the fields of medicinal chemistry and biochemistry may find this compound particularly useful for synthesizing novel pharmaceuticals or as a building block in drug discovery processes.

In addition to its applications in research, Acridine-9-carboxylic acid (6-amino-hexyl)amide can serve as a key intermediate in the synthesis of bioactive compounds, potentially leading to the development of new therapeutic agents. Its ability to interact with biological systems makes it a candidate for studies in cellular imaging and targeting. The compound's favorable properties, such as stability and reactivity, position it as a valuable tool for scientists looking to explore new avenues in drug development and molecular biology.

Synonyms
N-(6-Aminohexyl)acridine-9-carboxamide
CAS Number
259221-99-3
Molecular Formula
C20H23N3O
Molecular Weight
321.42
MDL Number
MFCD06658309
PubChem ID
10853218
Conditions
Store at 0-8°C
General Information
Synonyms
N-(6-Aminohexyl)acridine-9-carboxamide
CAS Number
259221-99-3
Molecular Formula
C20H23N3O
Molecular Weight
321.42
MDL Number
MFCD06658309
PubChem ID
10853218
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Acridine-9-carboxylic acid (6-amino-hexyl)amide is widely utilized in research focused on:

  • Drug Development: This compound serves as a scaffold in the synthesis of new pharmaceuticals, particularly in targeting cancer cells due to its ability to intercalate with DNA.
  • Fluorescent Probes: It is used to create fluorescent markers for biological imaging, helping researchers visualize cellular processes in real-time.
  • Antimicrobial Agents: The compound shows potential as an antimicrobial agent, making it valuable in developing treatments for infections.
  • Polymer Chemistry: It can be incorporated into polymer matrices to enhance properties such as thermal stability and mechanical strength, beneficial for materials science applications.
  • Bioconjugation: Acridine-9-carboxylic acid (6-amino-hexyl)amide can be used in bioconjugation techniques, aiding in the attachment of biomolecules to surfaces for biosensor development.

Citations