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Halichlorine

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Identification
Molecular formula
C24H35NO2
CAS number
141470-58-6
IUPAC name
5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-ol
State
State

At room temperature, Halichlorine is generally a solid. The structural complexity and specific stereochemistry of the compound confer enhanced stability in solid form under standard conditions. It remains as a crystalline solid at standard laboratory conditions of temperature and pressure.

Melting point (Celsius)
150.50
Melting point (Kelvin)
423.70
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
401.57g/mol
Molar mass
401.5690g/mol
Density
1.2100g/cm3
Appearence

The compound generally appears as a crystalline solid. However, due to its complexity, variations may exist depending on the form of the preparation. Purified samples can exhibit a range of colors from pale yellow to white.

Comment on solubility

Solubility of 5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-ol

The solubility of the compound 5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-ol (C24H35NO2) can be influenced by several factors, including its unique molecular structure and functional groups.

Key Factors Affecting Solubility:

  • Polarity: Polarity plays a crucial role as polar molecules tend to dissolve better in polar solvents. The presence of the hydroxyl group (-OH) gives this compound some degree of polarity, potentially enhancing solubility in polar solvents like water.
  • Hydrophobic Regions: The large hydrocarbon sections of the molecule suggest a hydrophobic character, which may hinder solubility in water but enhance solubility in organic solvents such as ethanol or methanol.
  • Temperature: Solubility may also increase with temperature; thus, heating the solvent may lead to a higher dissolution rate.

However, the overall solubility of this specific compound was not extensively documented in the literature, leaving its practical solubility characteristics somewhat open to exploration. Scientists often rely on experimental approaches to ascertain solubility in various media. As a general rule of thumb, it can be summarized that "like dissolves like"; hence, the context of the solvent choice is critical here.

In conclusion, the intricate interplay of the compound's structure with its environment demands further investigation to fully elucidate its solubility profile.

Interesting facts

Interesting Facts About 5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-ol

This compound, a fascinating member of the chemical world, showcases the intricate relationship between structure and function. Known for its unique spirocyclic framework, it represents a complex architecture of interconnected rings that can be particularly interesting for synthetic chemists and biochemists alike.

Key Highlights:

  • Complexity in Structure: The compound features a spiro connection, linking multiple cyclic structures in a single molecule, which can lead to diverse reactivity and interaction patterns.
  • Biological Relevance: Compounds like this often serve as potential candidates in drug discovery and medicinal chemistry, thanks to their structured frameworks and the presence of functional groups.
  • Versatile Synthesis: The synthesis of such complex compounds can involve various strategies, including multi-step organic synthesis, which hones the skills of chemists in designing and executing intricate synthetic routes.

Moreover, this compound's incorporation of oxygen in its ring structures enhances its potential interactions, making it a subject of interest in both materials science and pharmaceuticals. As a chemistry student, understanding the intricacies of such compounds can broaden your appreciation of molecular complexity and design.

In the words of renowned chemist Linus Pauling, "The best way to have a good idea is to have a lot of ideas." Exploring structures like this one is essential for nurturing creativity and innovation in chemistry!

With ongoing research, the potential applications and implications of 5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-ol continue to inspire chemists for future discoveries and advancements.

Synonyms
solasodine
Spirosol-5-en-3-ol
Salasdine
Salasodine
Purapuridine
126-17-0
Solancarpidine
Solasodin
Solanidine-S
Solancarpine
Sosasodine
Tomatidenol
Solanidine S
NSC179187
Solasod-5-en-3 beta-ol
Solasod-5-en-3.beta.-ol
SOLASODINE HYDROCHLORIDE BASE
Spirosol-5-en-3-ol,22.alpha.,25R)-
Solauricidine
NSC178260
NSC-179187
Solasod-5-en-3beta -ol
Oprea1_090106
CHEMBL1964743
SCHEMBL12838252
ACon1_001598
DTXSID40871610
Solasod-5-en-3alpha ,25R)-
SPIROSOL-5-EN-3-BETA-OL
BCP10954
AKOS003275084
NCGC00017170-02
DB-041812
(3|A,22|A,25R)-Spirosol-5-en-3-ol
Purapuridine; Solancarpidine; Solasodin; Salasdine
Spirosol-5-en-3-ol, (3beta ,22alpha ,25R)-
1415-77-6