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6-phenyl-1,2,3,4-tetrahydroisoquinolinium chloride

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Identification
Molecular formula
C15H16ClN
CAS number
NA
IUPAC name
6-phenyl-1,2,3,4-tetrahydroisoquinolin-2-ium;chloride
State
State

This compound is generally in a solid state at room temperature, often appearing as a crystalline solid.

Melting point (Celsius)
256.00
Melting point (Kelvin)
529.15
Boiling point (Celsius)
197.00
Boiling point (Kelvin)
470.15
General information
Molecular weight
309.82g/mol
Molar mass
309.8200g/mol
Density
1.2000g/cm3
Appearence

This compound typically appears as a white to off-white crystalline powder.

Comment on solubility

Solubility of 6-phenyl-1,2,3,4-tetrahydroisoquinolin-2-ium;chloride

The solubility of 6-phenyl-1,2,3,4-tetrahydroisoquinolin-2-ium;chloride in various solvents is an intriguing aspect of this compound.

Key Points on Solubility:

  • Solvent Interaction: This compound is likely to exhibit good solubility in polar solvents due to its ionic character stemming from the chloride.
  • Aqueous Solubility: It is expected to be soluble in water, as ions tend to interact favorably with water molecules.
  • Non-Polar Solvents: Solubility in non-polar solvents (such as hexane or benzene) is generally low, as the hydrophobic characteristics of the compound may limit its interaction with such solvents.
  • Temperature Dependence: Solubility may increase with temperature, which is a common behavior seen in many ionic compounds.

In summary, while 6-phenyl-1,2,3,4-tetrahydroisoquinolin-2-ium;chloride is expected to be soluble in water and other polar solvents, its solubility in non-polar environments remains limited. This behavior exemplifies the general principle of "like dissolves like," emphasizing the importance of solvent polarity in solubility chemistry.

Interesting facts

Interesting Facts about 6-Phenyl-1,2,3,4-tetrahydroisoquinolin-2-ium Chloride

6-Phenyl-1,2,3,4-tetrahydroisoquinolin-2-ium chloride is a fascinating compound that belongs to the family of isoquinolines, which are significant in both organic synthesis and medicinal chemistry. Here are some compelling points about this intriguing compound:

  • Structural Complexity: The compound features a tetrahydroisoquinoline structure that includes a phenyl substituent, contributing to its unique chemical properties and reactivity.
  • Biological Importance: Isoquinolines and their derivatives are noted for their diverse pharmacological activities, including anti-inflammatory, analgesic, and antitumor effects.
  • Research Applications: Compounds like 6-phenyl-1,2,3,4-tetrahydroisoquinolin-2-ium chloride are of interest in drug design and synthesis due to their potential for serving as scaffolds for developing new therapeutic agents.
  • Ion Formation: The chloride ion in this compound plays a crucial role in its interaction with biological systems, impacting solubility and permeability across cell membranes.
  • Potential Insights: Studies involving this compound may yield valuable information about neurotransmitter systems, especially considering its structural resemblance to naturally occurring brain neurochemicals.

In summary, 6-phenyl-1,2,3,4-tetrahydroisoquinolin-2-ium chloride is not only appealing due to its complex structure but also for its potential implications in science and medicine. As research progresses, it may reveal new pathways for pharmaceutical innovation and a deeper understanding of biological processes.

Synonyms
24464-11-7
DTXSID40947349
6-Phenyl-1,2,3,4-tetrahydroisoquinoline--hydrogen chloride (1/1)
RefChem:1074128
DTXCID101375609
6-Phenyl-1,2,3,4-tetrahydroisoquinoline hydrochloride
ISOQUINOLINE, 1,2,3,4-TETRAHYDRO-6-PHENYL-, HYDROCHLORIDE