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Catalog Number:
19285
CAS Number:
259221-98-2
Acridine-9-carboxylic acid (3-amino-propyl)amide
Synonym(s):
N-(3-Aminopropyl)acridine-9-carboxamide
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Product Information

Acridine-9-carboxylic acid (3-amino-propyl)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 biological activity, making it a valuable candidate in pharmaceutical research, particularly in the development of novel therapeutic agents. Its amide functionality enhances its solubility and bioavailability, which is crucial for drug formulation. Researchers have explored its use in synthesizing fluorescent probes and as a building block in organic synthesis, showcasing its adaptability in creating complex molecular architectures.

In addition to its pharmaceutical applications, Acridine-9-carboxylic acid (3-amino-propyl)amide has shown promise in the fields of materials science and biochemistry. Its ability to intercalate with nucleic acids opens avenues for its use in genetic research and diagnostics. The compound's unique properties make it an attractive option for researchers looking to develop innovative solutions in drug delivery systems and molecular imaging. With its multifaceted applications and beneficial characteristics, this compound stands out as a key player in advancing scientific research and industrial applications.

Synonyms
N-(3-Aminopropyl)acridine-9-carboxamide
CAS Number
259221-98-2
Molecular Formula
C17H17N3O
Molecular Weight
279.34
MDL Number
MFCD06658327
PubChem ID
10636391
Conditions
Store at 0-8°C
General Information
Synonyms
N-(3-Aminopropyl)acridine-9-carboxamide
CAS Number
259221-98-2
Molecular Formula
C17H17N3O
Molecular Weight
279.34
MDL Number
MFCD06658327
PubChem ID
10636391
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 (3-amino-propyl)amide is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceutical agents, particularly those targeting cancer and infectious diseases, enhancing drug efficacy.
  • Fluorescent Probes: Its unique structure allows it to be used in the development of fluorescent probes for biological imaging, aiding researchers in visualizing cellular processes.
  • Antimicrobial Applications: The compound exhibits antimicrobial properties, making it valuable in developing new antibacterial and antifungal agents, crucial for addressing resistance issues in medicine.
  • Material Science: It is utilized in creating advanced materials, such as polymers and coatings, that require specific optical and thermal properties, benefiting industries like electronics and packaging.
  • Biochemical Research: Researchers employ this compound in biochemical assays to study enzyme interactions and cellular functions, providing insights into metabolic pathways and disease mechanisms.

Citations