Interesting facts
Interesting Facts About 2,2-bis(4-chlorophenyl)ethanol
2,2-bis(4-chlorophenyl)ethanol, often referred to in the chemical community as BCP, is a compound that has garnered attention due to its unique structural properties and potential applications. Here are some intriguing insights about this molecule:
- Structural Composition: The molecule features two 4-chlorophenyl groups attached to a central ethanol unit, creating a significant degree of steric hindrance that influences its reactivity and interactions.
- Biological Activity: Research has indicated that BCP exhibits interesting biological properties, which may have implications in pharmacology. Its chlorinated phenyl groups can contribute to its efficacy in certain biological assays.
- Research Relevance: The compound is often studied for its role in the synthesis of more complex molecules, making it a valuable building block in organic chemistry.
- Environmental Considerations: Due to its chlorinated structure, the environmental stability and potential toxicity of BCP are critical areas of study. Understanding its behavior in various ecosystems is essential for assessing risks.
- Synthetic Pathways: BCP can be synthesized through various methods, including Friedel-Crafts alkylation, which highlights the versatility of chemical synthesis in creating chlorinated compounds.
In summary, 2,2-bis(4-chlorophenyl)ethanol is not only a fascinating compound from a structural standpoint but also offers a glimpse into broader applications within chemistry and environmental science. As we continue to explore its properties and effects, it remains a subject of interest for chemists and researchers alike.
Synonyms
2,2-Bis(4-chlorophenyl)ethanol
2642-82-2
2,2-BIS(P-CHLOROPHENYL)ETHANOL
2,2-Bis(4'-chlorophenyl)ethanol
DTXSID5041308
CHEBI:28410
NSC-8942
59856K2U1E
4-Chloro-beta-(4-chlorophenyl)benzeneethanol
DTXCID3021308
ZVIDYKRNLNAXFT-UHFFFAOYSA-
BIS(4-CHLOROPHENYL)ETHANOL, 2,2-
220-148-1
inchi=1/c14h12cl2o/c15-12-5-1-10(2-6-12)14(9-17)11-3-7-13(16)8-4-11/h1-8,14,17h,9h2
DDOH
p,p'-Ddoh
DDOM
2,2-Bis(4-chlorophenyl)-1-hydroxyethane
4,4'-DDOH
Ethanol, 2,2-bis(p-chlorophenyl)-
Benzeneethanol, 4-chloro-.beta.-(4-chlorophenyl)-
NSC 8942
Benzeneethanol, 4-chloro-beta-(4-chlorophenyl)-
Bis(p-chlorophenyl)ethanol
2,2-bis(4'-Chlorophenyl)ethanol (DDOH)
Caswell No. 091B
EINECS 220-148-1
BRN 2055080
UNII-59856K2U1E
2,2-bis(4-chlorophenyl)ethan-1-ol
Benzeneethanol,4-chloro-b-(4-chlorophenyl)-
bmse000671
4-06-00-04726 (Beilstein Handbook Reference)
SCHEMBL1979065
CHEMBL3182945
Ethanol,2-bis(p-chlorophenyl)-
NSC8942
2,2-Bis-(4-chloro-phenyl)ethanol
Tox21_300725
2,2-Bis-(4-chloro-phenyl)-ethanol
Ethanol, 2,2-bis-(4-chlorophenyl)
AKOS024307456
4,4'-DDOH, 99%
NCGC00248152-01
NCGC00254631-01
CAS-2642-82-2
DS-010149
NS00009353
C06639
4,4'-DDOH, PESTANAL(R), analytical standard
Q27103677
Solubility of 2,2-bis(4-chlorophenyl)ethanol
The solubility of 2,2-bis(4-chlorophenyl)ethanol, often abbreviated as bisphenol R, can be assessed based on its chemical structure and functional groups. Here are some key points regarding its solubility characteristics:
In summary, while 2,2-bis(4-chlorophenyl)ethanol exhibits some moderate solubility characteristics, its overall behavior is influenced by the nature of the solvent and environmental conditions such as temperature. Therefore, practical applications necessitate a thorough assessment of solubility in relevant solvents.