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Lysergic acid diethylamide

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Identification
Molecular formula
C20H25N3O
CAS number
50-37-3
IUPAC name
7-allyl-N,N-diethyl-6,6a,8,9-tetrahydro-4H-indolo[4,3-fg]quinoline-9-carboxamide
State
State
At room temperature, lysergic acid diethylamide is typically in the form of a crystalline solid.
Melting point (Celsius)
80.50
Melting point (Kelvin)
353.65
Boiling point (Celsius)
80.00
Boiling point (Kelvin)
353.15
General information
Molecular weight
323.45g/mol
Molar mass
323.4510g/mol
Density
1.0290g/cm3
Appearence

Lysergic acid diethylamide (commonly known as LSD) is typically encountered as a colorless, odorless crystalline substance. However, when used recreationally, it is often applied to blotter paper, which can be colorful and decorated.

Comment on solubility

Solubility of 7-allyl-N,N-diethyl-6,6a,8,9-tetrahydro-4H-indolo[4,3-fg]quinoline-9-carboxamide

The solubility of 7-allyl-N,N-diethyl-6,6a,8,9-tetrahydro-4H-indolo[4,3-fg]quinoline-9-carboxamide (C20H25N3O) can be described as follows:

  • Solvent Dependency: The solubility of this compound is highly dependent on the solvent used. It typically exhibits better solubility in organic solvents compared to polar solvents.
  • Polar vs Non-Polar: In non-polar solvents, such as benzene or dichloromethane, this compound tends to dissolve readily, whereas it may have limited solubility in water due to its hydrophobic structure.
  • Temperature Influence: Increasing the temperature often improves solubility, allowing for greater dissolution in suitable organic solvents.
  • Potential Applications: The solubility characteristics are crucial for its applications in pharmaceutical formulations, impacting bioavailability and efficacy.

In summary, the solubility of C20H25N3O is influenced by a variety of factors including the choice of solvent, temperature, and the compound's intrinsic properties. As such, it is essential to consider these aspects when planning experiments or applications involving this compound.

Interesting facts

Interesting Facts about 7-Allyl-N,N-Diethyl-6,6a,8,9-Tetrahydro-4H-Indolo[4,3-fg]quinoline-9-Carboxamide

The compound 7-allyl-N,N-diethyl-6,6a,8,9-tetrahydro-4H-indolo[4,3-fg]quinoline-9-carboxamide belongs to a unique class of organic molecules that exhibit a rich tapestry of potential applications and biological activities. Here are some engaging insights about this intriguing compound:

  • Structural Significance: The complex structure of this compound features a fused ring system that not only stabilizes the molecule but also enhances its biological activity. The presence of multiple functional groups contributes to its potential reactivity and interaction with biological systems.
  • Potential Biological Activity: Compounds of this class have been studied for their pharmacological properties. There is promise for use in medicinal applications, particularly due to their potential antibacterial, antifungal, and even anticancer activity. Their ability to interact with various biological targets makes them a subject of intense research.
  • Synthesis and Applications: The synthesis of such complex organic compounds often involves advanced techniques in organic chemistry, including multi-step synthetic routes and catalysis. Such synthetic methodologies not only highlight the ingenuity of chemists but also pave the way for the development of new therapeutic agents.
  • Novelty in Design: The design of compounds such as this one is rooted in the principles of medicinal chemistry, where variations in substitution patterns can lead to dramatically different pharmacokinetic and pharmacodynamic profiles. The exploration of such derivatives can lead to improved efficacy and reduced side effects in therapeutic contexts.

In conclusion, the study of 7-allyl-N,N-diethyl-6,6a,8,9-tetrahydro-4H-indolo[4,3-fg]quinoline-9-carboxamide illustrates the delicate balance between structure and function in chemical compounds. As researchers delve into the potential of these molecular architectures, exciting discoveries await that may one day lead to new treatments and technologies.

Synonyms
AL-LAD (solution)
6-Nor-allyl-lysergic acid diethylamide
JCQLEPDZFXGHHQ-UHFFFAOYSA-N
6-Allyl-N,N-diethyl-9,10-didehydroergoline-8-carboxamide #
7-allyl-N,N-diethyl-4,6,6a,7,8,9-hexahydroindolo[4,3-fg]quinoline-9-carboxamide