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2-CDE Phenethylamine hydrochloride

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Identification
Molecular formula
C8H11Cl3NO
CAS number
.null
IUPAC name
[2-(3,4-dichlorophenyl)-2-hydroxy-ethyl]ammonium;chloride
State
State

At room temperature, 2-CDE Phenethylamine hydrochloride is in a solid state.

Melting point (Celsius)
215.00
Melting point (Kelvin)
488.15
Boiling point (Celsius)
150.50
Boiling point (Kelvin)
423.70
General information
Molecular weight
268.60g/mol
Molar mass
268.6000g/mol
Density
1.3000g/cm3
Appearence

2-CDE Phenethylamine hydrochloride typically appears as a white to off-white crystalline solid.

Comment on solubility

Solubility of [2-(3,4-dichlorophenyl)-2-hydroxy-ethyl]ammonium;chloride

The solubility of [2-(3,4-dichlorophenyl)-2-hydroxy-ethyl]ammonium;chloride in various solvents can be quite interesting due to its unique structural components. Here are some key points about its solubility:

  • Water Solubility: This compound tends to be soluble in water, primarily due to the presence of the ammonium group which can readily interact with water molecules.
  • Solvent Compatibility: It is likely to show differing solubility in organic solvents. For instance, when considering solvents such as ethanol or methanol, the overall solubility might vary as hydrogen bonding plays a crucial role.
  • Influencing Factors: Factors such as temperature, pH levels, and the ionic strength of the solution can significantly affect its solubility. Generally, increased temperature tends to enhance solubility for most salts.
  • Structural Dynamics: The bulky chlorophenyl group may influence the steric hindrance around the ammonium central atom, further impacting its interaction with solvent molecules.

In summary, the solubility behavior of [2-(3,4-dichlorophenyl)-2-hydroxy-ethyl]ammonium;chloride cannot be generalized. It is essential to examine individual solvent interactions and environmental conditions to fully understand its solubility characteristics. This complexity adds to its fascinating chemical profile.

Interesting facts

Interesting Facts about [2-(3,4-Dichlorophenyl)-2-Hydroxy-Ethyl]ammonium; Chloride

[2-(3,4-Dichlorophenyl)-2-Hydroxy-Ethyl]ammonium; chloride is a fascinating compound that combines elements of organic chemistry with potential applications in various fields, including pharmaceuticals and chemical research.

Key Highlights:

  • Pharmaceutical Relevance: Due to its chemical structure, this compound may exhibit significant biological activity, which can be explored for development in drugs targeting specific diseases.
  • Mechanism of Action: Compounds like this one can act as modulators of various physiological processes, potentially influencing neurotransmitter systems or other biochemical pathways.
  • Structure-Activity Relationship (SAR): The presence of the dichlorophenyl group suggests a unique interaction with biological targets, which researchers can study to optimize its efficacy and reduce side effects.
  • Environmentally Relevant: The environmental impact of such compounds can be critical, as their stability and degradation products can raise concerns during their production and use.
  • Research Opportunities: The compound presents numerous avenues for scientific exploration, ranging from its synthesis and characterization to investigating its reactivity and potential use in catalysis.

As science continues to advance, compounds like [2-(3,4-Dichlorophenyl)-2-Hydroxy-Ethyl]ammonium; chloride will play a crucial role in the drive towards innovative solutions in both health and environmental sustainability. Further investigation into such compounds helps expand our understanding of their properties and opportunities for practical application.

Synonyms
alpha-(Aminomethyl)-3,4-dichlorobenzyl alcohol hydrochloride
3672-26-2
alpha-3,4-Dichlorophenyl-beta-aminoethanol hydrochloride
Benzenemethanol, alpha-(aminomethyl)-3,4-dichloro-, hydrochloride
BENZYL ALCOHOL, alpha-(AMINOMETHYL)-3,4-DICHLORO-, HYDROCHLORIDE
[2-(3,4-dichlorophenyl)-2-hydroxyethyl]azanium chloride
DB-249290
[2-(3,4-dichlorophenyl)-2-hydroxyethyl]azanium;chloride