209414-06-2

Basic information

• Product Name: 1-Naphthalenyl(1-propyl-1H-indol-3-yl)methanone
• Synonyms: 1-Naphthalenyl(1-propyl-1H-indol-3-yl)methanone;naphthalen-1-yl(1-propyl-1H-indol-3-yl)Methanone;JWH 072
• CAS NO: 209414-06-2
• Molecular Formula: C22H19NO
• Molecular Weight: 313.39
• Mol File: 209414-06-2.mol

Chemical Properties

• Boiling Point: 515.549 °C at 760 mmHg
• Flash Point: 265.595 °C
• Appearance: /
• Density: 1.11
• CAS DataBase Reference: 1-Naphthalenyl(1-propyl-1H-indol-3-yl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Naphthalenyl(1-propyl-1H-indol-3-yl)methanone(209414-06-2)
• EPA Substance Registry System: 1-Naphthalenyl(1-propyl-1H-indol-3-yl)methanone(209414-06-2)

Safety Data

• Hazardous Substances Data: 209414-06-2(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Research:
1-Naphthalenyl(1-propyl-1H-indol-3-yl)methanone is used as a research compound for its potential pharmacological properties. Its unique structure allows it to interact with specific biological targets, making it a valuable tool in the development of new drugs and therapies.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 1-Naphthalenyl(1-propyl-1H-indol-3-yl)methanone is used as a lead compound for the design and synthesis of novel therapeutic agents. Its structural features can be modified to optimize its biological activity and selectivity, potentially leading to the discovery of new drugs with improved efficacy and safety profiles.
Used in Cannabinoid Research:
1-Naphthalenyl(1-propyl-1H-indol-3-yl)methanone, being a synthetic indole derivative, may also be used in the study of cannabinoid receptors, such as the CB2 receptor. As a CB2 receptor agonist, it can provide insights into the role of these receptors in various physiological processes and may contribute to the development of targeted therapies for conditions related to the endocannabinoid system.