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AH7921 hydrochloride

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Identification
Molecular formula
C17H21ClNO
CAS number
851202-83-0
IUPAC name
1,2-diphenyl-2-piperidin-1-ium-1-yl-ethanone;chloride
State
State

AH7921 hydrochloride is typically in a solid state at room temperature. The compound is stable and should be stored in a cool, dry place to maintain its integrity.

Melting point (Celsius)
187.00
Melting point (Kelvin)
460.15
Boiling point (Celsius)
260.00
Boiling point (Kelvin)
533.15
General information
Molecular weight
364.91g/mol
Molar mass
364.9100g/mol
Density
1.1000g/cm3
Appearence

AH7921 hydrochloride appears as a white or off-white crystalline powder. The substance is typically found in a solid state at room temperature.

Comment on solubility

Solubility of 1,2-Diphenyl-2-piperidin-1-ium-1-yl-ethanone Chloride

The solubility of the compound 1,2-diphenyl-2-piperidin-1-ium-1-yl-ethanone chloride can be quite interesting and is influenced by various factors such as its ionic nature, molecular structure, and environmental conditions. Here are some key points to consider:

  • Solubility Type: As a quaternary ammonium compound, the chloride salt form typically exhibits good solubility in polar solvents.
  • Solvent Compatibility: It is likely to dissolve well in water and other protic solvents due to its ionic characteristics.
  • Temperature Effects: Solubility may increase with temperature, allowing for a higher degree of dissolution in solvents.
  • Environmental Influence: Factors such as pH and ionic strength of the solution can significantly affect solubility.

In conclusion, the solubility of 1,2-diphenyl-2-piperidin-1-ium-1-yl-ethanone chloride makes it an interesting candidate for applications in various chemical reactions and formulations. Its ability to dissolve in polar solvents allows for flexibility in its use in both laboratory and industrial settings.

Interesting facts

Interesting Facts about 1,2-Diphenyl-2-piperidin-1-ium-1-yl-ethanone; Chloride

1,2-Diphenyl-2-piperidin-1-ium-1-yl-ethanone; chloride is a fascinating compound, not just because of its intricate structure but also due to its multifaceted applications and implications in the field of chemistry.

Key Applications

  • Pharmaceutical Research: This compound plays a significant role in the development of new medicinal agents, particularly in the study of anti-inflammatory and analgesic properties.
  • Ligand Chemistry: It serves as a ligand in coordination chemistry, aiding in the synthesis of metal complexes which are essential in catalysis.
  • Organic Synthesis: Its unique structure allows chemists to utilize it in various organic reactions, enhancing synthesis pathways for complex molecules.

Significant Chemical Properties

The presence of both a piperidine ring and phenyl groups in this compound grants it interesting electronic properties, enabling diverse interactions in different environments. The piperidine provides a nitrogen atom that can participate in hydrogen bonding, while the phenyl groups can stabilize reactive intermediates through resonance.

Historical Context

This compound exemplifies the breadth of organic chemistry and highlights how intricate variations in structure can lead to vastly different properties and functions. Notably, structures similar to this compound have been explored since the mid-20th century, reflecting decades of research aimed at understanding their potential.

Thoughts from Chemists

As one chemist once remarked, "In the enigmatic world of molecular structures, each compound tells a story of possibility and innovation." This sentiment rings especially true for 1,2-diphenyl-2-piperidin-1-ium-1-yl-ethanone; chloride, whose potential applications continue to inspire and challenge researchers today.

In conclusion, 1,2-diphenyl-2-piperidin-1-ium-1-yl-ethanone; chloride is not just a chemical substance but a key player in the ongoing quest for new discoveries in both academia and industry.

Synonyms
Phenyl alpha-piperidinobenzyl ketone hydrochloride
6281-83-0
NSC 5898
NSC 40313
2-Phenyl-2-piperidinoacetophenone hydrochloride
Ketone, phenyl alpha-piperidinobenzyl, hydrochloride
ACETOPHENONE, 2-PHENYL-2-PIPERIDINO-, HYDROCHLORIDE
Ethanone, 1,2-diphenyl-2-(1-piperidinyl)-, hydrochloride