Interesting facts
Interesting Facts about 4,4-Diphenyl-6-(1-piperidyl)heptan-3-one
4,4-Diphenyl-6-(1-piperidyl)heptan-3-one is an intriguing compound within the vast field of organic chemistry, and it offers several points of interest for students and researchers alike. Here are a few notable aspects:
- Pharmacological Relevance: This compound is classified as a piperidine derivative. Compounds containing a piperidine ring are known for their diverse biological activities, including potential applications in the pharmaceutical industry.
- Synthetic Versatility: The structure of 4,4-diphenyl-6-(1-piperidyl)heptan-3-one provides opportunities for various synthetic modifications. As a result, chemists can explore different derivatives, leading to the discovery of new compounds with unique properties.
- Structural Features: The presence of multiple phenyl groups in its structure not only contributes to its stability but also enhances its interactions with biological targets, making it a compound of interest in medicinal chemistry.
- Research Applications: Given its unique functional groups, 4,4-diphenyl-6-(1-piperidyl)heptan-3-one can serve as a starting point for the synthesis of compounds aimed at studying the central nervous system or for developing new analgesics.
In conclusion, 4,4-diphenyl-6-(1-piperidyl)heptan-3-one exemplifies the rich potential present in organic compounds. Its engaging structural characteristics and promising applications in drug development make it a valued subject of study in modern chemistry.
Synonyms
DIPIPANONE
Piperidylamidone
Phenylpiperon
Dipipanona
Pipadone
phenylpiperone
Dipipanonum
Dipipanon
4,4-Diphenyl-6-piperidino-3-heptanone
Piperidyl-amidon
Piperidyl-methadon
Dipipanone [INN:BAN]
Acscn-9622
Dipipanonum [INN-Latin]
Piperidyl amidone
Dipipanona [INN-Spanish]
Pamedon(e)
IDS-ND-017
UNII-X188638Y2V
DIPIPANONE [MI]
DIPIPANONE [INN]
EINECS 207-399-2
3-Heptanone, 4,4-diphenyl-6-(1-piperidinyl)-
X188638Y2V
DIPIPANONE [WHO-DD]
3-Heptanone, 4,4-diphenyl-6-piperidino-
dl-4,4-diphenyl-6-piperidinoheptan-3-one
Hoechst 10805 (Salt/Mix)
378 C 48 (Salt/Mix)
DTXSID50894759
Dipipanone hydrochloride (Salt/Mix)
Diconal tablets (dipipanone+cyclizine)
Dipipanonum (INN-Latin)
Dipipanona (INN-Spanish)
4,4-di(phenyl)-6-piperidin-1-ylheptan-3-one
6-PIPERIDINO-4,4-DIPHENYLHEPTAN-3-ONE
2-(1-PIPERIDINO)-4,4-DIPHENYL-5-HEPTANONE
DTXCID301324321
4,4-diphenyl-6-(piperidin-1-yl)heptan-3-one
207-399-2
svdhszfeqyxrdc-uhfffaoysa-n
467-83-4
4,4-diphenyl-6-piperidin-1-ylheptan-3-one
Dipipanone (BAN)
SCHEMBL25367
GTPL9081
DEA No. 9622
CHEMBL2111157
CHEBI:135479
HY-U00328
CS-7346
DB01491
NS00044169
D12671
4,4-Diphenyl-6-(1-piperidinyl)-3-heptanone #
Q4162039
piperidine, 1-(3-ethylcarbonyl-1-methyl-3,3-diphenyl)propyl-
Solubility of 4,4-Diphenyl-6-(1-piperidyl)heptan-3-one
The solubility of 4,4-diphenyl-6-(1-piperidyl)heptan-3-one can be categorized based on its structural characteristics, which influence its interaction with solvents. Generally, this compound exhibits the following solubility behaviors:
As a general rule in organic chemistry, "Like dissolves like," meaning that non-polar compounds tend to dissolve in non-polar solvents. Conversely, polar compounds prefer polar solvents. Therefore, with the combination of both polar (piperidyl moiety) and non-polar (phenyl groups) characteristics, appropriate solvent selection is crucial for optimal solubility.
In summary, understanding the solubility characteristics of 4,4-diphenyl-6-(1-piperidyl)heptan-3-one can significantly aid in its application in various chemical processes. Remember that solubility can play a critical role in reactions, extraction processes, and pharmaceutical formulations.