Interesting facts
Interesting Facts about 1-Phenylpentan-1-ol
1-Phenylpentan-1-ol is an intriguing organic compound with various applications and characteristics that make it noteworthy in the field of chemistry. Here are some fascinating insights into this compound:
- Structural Features: This compound features a long carbon chain, which contributes to its stability and unique properties. The presence of both a phenyl group and a hydroxyl group makes it a primary alcohol.
- Synthesis: 1-Phenylpentan-1-ol can be synthesized through several methods, with one common approach being the reaction of phenylmagnesium bromide with an appropriate aldehyde. This showcases the compound’s versatility in organic synthesis.
- Applications: The compound is often explored for its potential use in chemical synthesis and may serve as an intermediate for various pharmaceutical products. Its alcohol functional group also suggests possible applications as a solvent or in the fragrance industry.
- Functional Group Characteristics: The presence of the hydroxyl (-OH) group is significant; it can engage in hydrogen bonding, influencing the compound’s reactivity and interaction with other substances. This property is critical when considering the compound's solubility and reactivity with acids and bases.
- Potential Research Interest: Researchers continually explore compounds like 1-phenylpentan-1-ol for their biological activities, which may open doors to novel medicinal applications or enhance existing substances’ effectiveness.
In summary, 1-phenylpentan-1-ol stands out not only due to its structural and functional attributes but also because of its diverse applications in various fields. It's examples like these that highlight the intricate balance of structure and function in organic chemistry, reminding us of the complex chemistry underlying everyday materials.
Synonyms
fenipentol
1-phenylpentan-1-ol
1-Phenyl-1-pentanol
583-03-9
Pancoral
1-Phenylpentanol
Phenylbutylcarbinol
alpha-Butylbenzyl alcohol
Suiclisin
1-Pentanol, 1-phenyl-
1-Phenyl-1-hydroxypentane
PH BC
Fenipentolum
1-Hydroxy-1-phenylpentane
Benzenemethanol, .alpha.-butyl-
Fenipentol [INN:JAN]
alpha-Butylbenzenemethanol
Fenipentolum [INN-Latin]
.alpha.-Butylbenzyl alcohol
NSC 8478
1-phenyl-1-hydroxy-n-pentane
PC 1
Benzyl alcohol, .alpha.-butyl-
PH-BC
NSC-8478
EINECS 209-493-9
Benzenemethanol, alpha-butyl-
BRN 1908761
X3FZE77O60
DTXSID4046818
AI3-36514
BENZYL ALCOHOL, alpha-BUTYL-
FENIPENTOL [MI]
FENIPENTOL [INN]
FENIPENTOL [JAN]
FENIPENTOL [MART.]
.alpha.-Butylbenzenemethanol
FENIPENTOL [WHO-DD]
DTXCID2026818
4-06-00-03371 (Beilstein Handbook Reference)
(+/-)-1-PHENYL-1-PENTANOL
(+/-)-.ALPHA.-BUTYLBENZYL ALCOHOL
Fenipentolum (INN-Latin)
FENIPENTOL (MART.)
fenipentolo
UNII-X3FZE77O60
NCGC00181036-01
a-ButylbenzylAlcohol
MFCD00021935
n-Butyl phenyl carbinol
1-Phenyl-pentan-1-ol
Fenipentol (JAN/INN)
1-PHNP
SCHEMBL21837
CHEMBL2104321
CHEBI:31600
NSC8478
HMS3713L06
AAA58303
HY-B1273
UAA64153
Tox21_112684
s5702
AKOS009158098
CCG-213901
(+/-)-ALPHA-BUTYLBENZYL ALCOHOL
NCGC00344546-01
AS-76425
CAS-583-03-9
DA-53152
CS-0013053
NS00008854
P1086
D01751
D89432
D92069
EN300-128588
AB01563209_01
A831823
Q426345
SR-01000944264
SR-01000944264-1
BRD-A66284731-001-01-2
BRD-A66284731-001-02-0
209-493-9
Solubility of 1-phenylpentan-1-ol (C11H16O)
1-phenylpentan-1-ol is an organic compound characterized by its distinct alcohol functional group, which significantly influences its solubility properties. This compound presents an intriguing solubility profile owing to its molecular structure, which consists of a long hydrocarbon chain that is substituted with a phenyl group.
Key Points on Solubility:
In conclusion, while 1-phenylpentan-1-ol can dissolve to some extent in aqueous solutions, its primary solubility will be prominent in non-polar organic solvents, demonstrating an essential aspect of its chemical behavior.