Interesting facts
Interesting Facts about 2-Aminocyclohexanol
2-Aminocyclohexanol is an intriguing compound with a variety of applications and properties that make it worthwhile for both scientists and students to explore. Here are some fascinating insights:
- Structural Complexity: This compound features a cyclic structure with an amine group, which significantly influences its chemical behavior and interactions. The presence of both an amino and hydroxyl group provides unique reactivity opportunities, particularly in organic synthesis.
- Applications in Synthesis: 2-Aminocyclohexanol is often utilized as an intermediate in the production of pharmaceuticals and agrochemicals. Its ability to serve as a chiral building block makes it particularly valuable in asymmetric synthesis.
- Biological Relevance: Compounds with amino and alcohol functional groups are common in biological systems. Studying 2-aminocyclohexanol can lead to a better understanding of biological pathways and molecular mechanisms in living organisms.
- Research Potential: Due to its unique structure, this compound is frequently investigated for its potential as a ligand in coordination chemistry and catalysis, making it a subject of ongoing research. Scientists are keen to explore how modifications to the amino or hydroxyl group can influence its reactivity.
- Teaching Tool: For chemistry students, 2-aminocyclohexanol serves as an excellent example of stereochemistry and functional group chemistry, providing a hands-on understanding of reaction mechanisms and molecular interactions.
In summary, 2-aminocyclohexanol is not merely a chemical compound; it is a gateway to exploring deeper concepts in organic and biological chemistry. Its diverse applications and structural uniqueness make it a compound worthy of study in both academic and industrial settings.
Synonyms
2-aminocyclohexan-1-ol
PQMCFTMVQORYJC-UHFFFAOYSA-
640-699-5
inchi=1/c6h13no/c7-5-3-1-2-4-6(5)8/h5-6,8h,1-4,7h2
2-AMINOCYCLOHEXANOL
6850-38-0
1-Amino-2-hydroxycyclohexane
931-15-7
Cyclohexanol, 2-amino-, cis-
cis-2-Amino-cyclohexanol
2-Aminocyclohenxanol
2-Aminocyclohexanol (cis- and trans- mixture)
2-amino-1-cyclohexanol
2-AMINO-CYCLOHEXANOL
(1S, 2S)-2-Aminocyclohexanol
Cyclohexanol, 2-amino-
Cyclohexanol,2-amino-,trans-
cyclohexane, 1-amino-2-hydroxy-
MFCD12407412
rel-(1R,2R)-2-Aminocyclohexan-1-ol
Cyclohexanol, 2-amino-, (1R,2S)-rel-
2-amino cyclohexanol
MFCD00191368
NoName_3025
2-azanylcyclohexan-1-ol
(+/-)-2-aminocyclohexanol
SCHEMBL64727
cis-2-Hydroxycyclohexaneamine
2-Aminocyclohexanol, AldrichCPR
(1S,2R)-2-Amino-cyclohexanol
DTXSID60902516
rel-(1R,2S)-2-Aminocyclohexanol
MFCD17976458
AKOS009156838
AB15074
AB49860
PB42414
PS-4141
SB40857
SB45208
SY026110
SY026111
SY029165
SY056778
A1258
CS-0128497
EN300-62225
A844450
Solubility of 2-aminocyclohexanol
2-aminocyclohexanol, a compound characterized by its amine and hydroxyl functional groups, exhibits notable solubility properties. Here are some key points regarding its solubility:
In summary, “2-aminocyclohexanol’s solubility is primarily attributed to its polar functional groups, which facilitate interactions with water and other polar solvents.” Understanding these solubility properties is crucial for practical applications in various fields, including pharmaceuticals and chemical synthesis.