Interesting facts
Interesting Facts about 2-(1-piperidyl)ethyl 2-hydroxy-2,2-diphenyl-acetate
The compound 2-(1-piperidyl)ethyl 2-hydroxy-2,2-diphenyl-acetate, often abbreviated in various contexts, is a fascinating compound praised for its diverse applications. Below are some intriguing details about this compound:
- Pharmaceutical Relevance: This compound can be explored for its potential therapeutic applications, particularly in the fields of psychiatry and neurology. Research indicates it may possess properties conducive to affecting neurotransmitter pathways.
- Structural Versatility: With features such as a piperidine ring and multiple phenyl groups, this compound exhibits structural properties that allow for intriguing interactions within biological systems.
- Chirality Considerations: The presence of chiral centers in its structure can lead to different biological activities of its enantiomers, making stereochemistry an important aspect of its study.
- Synthetic Pathways: Scientists have devised various synthetic routes for this compound, showcasing the ingenuity involved in chemical synthesis, which has significant implications for medicinal chemistry and materials science.
As a future chemist or an enthusiast in organic synthesis, understanding the nuances and applications of compounds like 2-(1-piperidyl)ethyl 2-hydroxy-2,2-diphenyl-acetate not only contributes to the expansion of chemical knowledge but also enhances our ability to innovate in drug development.
In the words of renowned chemist Linus Pauling, “The best way to have a good idea is to have lots of ideas.” Exploring compounds like this one is a critical step in fueling creativity and discovery in the world of chemistry.
Synonyms
Piperilate
Pipethanate
4546-39-8
Pipetanato
Pipethanate [INN]
1-Piperidineethanol benzilate
2-piperidin-1-ylethyl 2-hydroxy-2,2-diphenylacetate
2-(1-Piperidino)ethyl benzilate
BENZILIC ACID, 2-PIPERIDINOETHYL ESTER
P32MG14U83
Pipethanate (INN)
Pipethanatum
Pipetanato [INN-Spanish]
Pipethanatum [INN-Latin]
beta-Piperidylethyl benzilate
Pipethanate; beta-Piperidylethyl benzilate
NCGC00181083-01
BRN 0385167
UNII-P32MG14U83
PIPERILATE [MI]
alpha-Hydroxy-alpha-phenylbenzeneacetic acid 2-(1-piperidinyl)ethyl ester
Benzeneacetic acid, alpha-hydroxy-alpha-phenyl-, 2-(1-piperidinyl)ethyl ester
SCHEMBL26493
PIPETHANATE [WHO-DD]
4-20-00-00432 (Beilstein Handbook Reference)
.beta.-Piperidylethyl benzilate
CHEMBL1722893
DTXSID2023484
CHEBI:135438
ALBB-035677
AKOS040766803
Pipethanate; -Piperidylethyl benzilate
Benzeneacetic acid, .alpha.-hydroxy-.alpha.-phenyl-, 2-(1-piperidinyl)ethyl ester
DA-56886
HY-105790
CS-0026650
2-piperidin-1-ylethyl hydroxy(diphenyl)acetate
D08384
Q27286058
Z242913010
2-piperidin-1-ylethyl hydroxy(diphenyl)acetate hydrochloride
.ALPHA.-HYDROXY-.ALPHA.-PHENYL-, 2-(1-PIPERIDINYL)ETHYL ESTER
.alpha.-Hydroxy-.alpha.-phenylbenzeneacetic acid 2-(1-piperidinyl)ethyl ester
Solubility of 2-(1-piperidyl)ethyl 2-hydroxy-2,2-diphenyl-acetate
The solubility of 2-(1-piperidyl)ethyl 2-hydroxy-2,2-diphenyl-acetate can be influenced by several factors. This compound, which contains both hydrophilic and hydrophobic functional groups, exhibits intriguing solubility characteristics:
In summary, while the solubility can vary based on environmental conditions, one might expect 2-(1-piperidyl)ethyl 2-hydroxy-2,2-diphenyl-acetate to display relatively higher solubility in non-polar organic solvents and limited solubility in polar solvents. Understanding these solubility properties is essential for its application in various chemical and pharmaceutical contexts.