6,7-Dimethoxy-1-pentyl-1,2,3,4-tetrahydroisoquinoline

Identification

Molecular formula

C₁₆H₂₅NO₂

CAS number

22347-41-1

IUPAC name

6,7-dimethoxy-1-pentyl-1,2,3,4-tetrahydroisoquinoline

State

The compound is in a solid state at room temperature. It is typically stable in air and under standard laboratory conditions.

Melting point (Celsius)

79.00

Melting point (Kelvin)

352.15

Boiling point (Celsius)

355.00

Boiling point (Kelvin)

628.15

General information

Molecular weight

277.38g/mol

Molar mass

277.4030g/mol

Density

1.0750g/cm³

Appearence

6,7-dimethoxy-1-pentyl-1,2,3,4-tetrahydroisoquinoline typically appears as a pale yellow or off-white crystalline solid. It may also be available as a powder, and its appearance can vary slightly depending on its level of purity.

Comment on solubility

Solubility of 6,7-dimethoxy-1-pentyl-1,2,3,4-tetrahydroisoquinoline

The solubility characteristics of 6,7-dimethoxy-1-pentyl-1,2,3,4-tetrahydroisoquinoline are fascinating and reveal important insights into the compound's behavior in various environments. This organic compound, featuring a complex molecular structure, is influenced by several factors when it comes to solubility:

Polarity: The presence of methoxy groups contributes to the overall polarity of the molecule, which can enhance its solubility in polar solvents such as water or alcohol.
Hydrophobic character: The pentyl side chain adds hydrophobic characteristics, which may promote solubility in non-polar solvents like hexane or toluene.
Temperature effects: Solubility may increase with temperature, as higher temperatures generally provide energy that can help break intermolecular interactions.

In summary, the solubility of this compound can vary significantly depending on the solvent and environmental conditions. It is essential for researchers and chemists to consider these factors when working with 6,7-dimethoxy-1-pentyl-1,2,3,4-tetrahydroisoquinoline, as they can greatly influence both its application and stability.

Interesting facts

Interesting Facts About 6,7-Dimethoxy-1-pentyl-1,2,3,4-tetrahydroisoquinoline

6,7-Dimethoxy-1-pentyl-1,2,3,4-tetrahydroisoquinoline is a fascinating compound that belongs to the class of isoquinolines, which are known for their wide range of biological activities. Here are some intriguing facts about this compound:

Structural Uniqueness: The inclusion of a tetrahydroisoquinoline core, modified with two methoxy groups and a pentyl chain, gives this molecule a unique structural framework. This structure can offer interesting interactions with biological targets.
Biological Significance: Isoquinoline derivatives, including this compound, are renowned for their various pharmacological properties, such as anti-inflammatory, analgesic, and neuroprotective effects. Research into compounds like this one can shed light on new therapeutic avenues.
Psychoactive Research: Compounds with a similar structural motif have been studied in the context of psychoactive effects. The presence of the pentyl substituent may enhance its ability to cross the blood-brain barrier, making it a topic of interest for neuropharmacological studies.
Potential Synthesis Pathways: Chemists are excited about the synthesis of such compounds, as they often involve innovative methods that push the boundaries of organic chemistry. Methods include various alkylation and substitution reactions to achieve the desired functionality.
Relevance in Natural Products: Isoquinolines are commonly found in many natural sources, including plants and fungi. This compound could potentially be isolated from natural extracts or synthesized in the lab for further study.

Overall, 6,7-dimethoxy-1-pentyl-1,2,3,4-tetrahydroisoquinoline represents a compelling subject of study in the realm of medicinal chemistry, with the potential to unlock new therapeutic possibilities.

Synonyms

22895-75-6

1-Pentyl-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline

SCHEMBL28017876