Interesting facts
Interesting Facts about Bis(4-chlorophenyl)-cyclopropyl-methanol
Bis(4-chlorophenyl)-cyclopropyl-methanol is a fascinating compound that has attracted attention in both industrial and academic circles due to its unique structure and potential applications. Here are some intriguing points about this compound:
- Chemical Structure: This compound features a cyclopropyl group, known for its strain and reactivity. The presence of two 4-chlorophenyl groups enhances its lipophilicity, which can influence its interactions in biological systems.
- Biological Activity: Compounds featuring cyclopropyl moieties often exhibit interesting pharmacological properties. There is ongoing research into the potential effectiveness of this compound in drug development, particularly in targeting specific biological pathways.
- Synthetic Routes: The synthesis of bis(4-chlorophenyl)-cyclopropyl-methanol can include various methodologies, making it a subject of study for chemists interested in reaction mechanisms and organic synthesis techniques.
- Applications in Material Science: The unique properties of cyclopropane derivatives can lead to applications in the development of new materials, such as polymers with specific mechanical properties, or as precursors for more complex chemical structures.
- Environmental Considerations: Understanding the environmental impact of synthetic compounds like this is critical. Studies often focus on their biodegradability and toxicity in various ecosystems.
In summary, due to its distinctive structural features and potential implications in various fields such as medicinal chemistry and materials science, bis(4-chlorophenyl)-cyclopropyl-methanol remains a compound of significant interest among chemists and researchers alike.
Synonyms
Proclonol
14088-71-2
Proclonolum
R 8284
2IGW7XIE2Y
R-8284
DTXSID4057972
bis(4-chlorophenyl)cyclopropylmethanol
Benzenemethanol, 4-chloro-alpha-(4-chlorophenyl)-alpha-cyclopropyl-
DTXCID2031740
237-934-5
Kilacar
Dupont DPX 3654
Bis(p-chlorophenyl)cyclopropylmethanol
bis(4-chlorophenyl)-cyclopropylmethanol
DPX 3654
CL 69049
Kilacar; R 8284
METHANOL, BIS(p-CHLOROPHENYL)CYCLOPROPYL-
Bis(4-chlorophenyl)(cyclopropyl)methanol
Benzenemethanol, 4-chloro-.alpha.-(4-chlorophenyl)-.alpha.-cyclopropyl-
Proclonolum [INN-Latin]
CCRIS 7252
EINECS 237-934-5
UNII-2IGW7XIE2Y
Bis-p-chlorophenyl cyclopropyl methanol
BRN 3324205
Proclono
Proclonol [USAN:INN:BAN]
AI3-27447
PROCLONOL [INN]
Proclonol (USAN/INN)
PROCLONOL [USAN]
SCHEMBL162595
orb1701767
CHEMBL2105277
CHEBI:229921
Di(p-Chlorophenyl)cyclopropylmethanol
Bis(p-chlorophenyl)cyclopropylcarbinol
AKOS040747307
Bis(4-chlorophenyl)(cyclopropyl)methanol #
CS-0068838
NS00024568
D05617
SR-01000945075
4,4'-DICHLORO-.ALPHA.-CYCLOPROPYLBENZHYDROL
SR-01000945075-1
Q27254787
4-CHLORO-.ALPHA.-(4-CHLOROPHENYL)-.ALPHA.-CYCLOPROPYLBENZENEMETHANOL
Solubility of Bis(4-chlorophenyl)-cyclopropyl-methanol
When examining the solubility of bis(4-chlorophenyl)-cyclopropyl-methanol, several factors come into play that influence its behavior in solvents. This compound, characterized by its unique structure, can exhibit:
Overall, bis(4-chlorophenyl)-cyclopropyl-methanol demonstrates variable solubility depending on the solvent choice. It raises the question: “What solvent conditions will best allow this compound to dissolve effectively?” Generally, the ability to dissolve in a particular solvent is essential for understanding its potential applications in chemical processes.
In summary, the solubility profile of this compound suggests that while it may not be highly soluble in aqueous solutions, an organic solvent would likely create a more favorable environment for dissolution.
Always consider the balance between polar and non-polar attributes when assessing solubility!