Interesting facts
Interesting Facts about 8,8-Dimethoxy-2,6-Dimethyl-Octan-2-ol
8,8-Dimethoxy-2,6-dimethyl-octan-2-ol is a fascinating compound that showcases the diversity and complexity of organic chemistry. Here are some captivating facts about this unique molecule:
- Structural Overview: This compound features a long hydrocarbon chain with multiple functional groups, making it an intriguing subject of study in terms of chemical reactivity and properties. Its structure includes both hydroxyl (-OH) and methoxy (-OCH3) groups, which significantly influence its chemical behavior.
- Applications: Compounds like 8,8-dimethoxy-2,6-dimethyl-octan-2-ol may find applications in various fields, such as:
- Pharmaceuticals: Potential precursors in the synthesis of therapeutic agents.
- Fragrance Industry: Serving as a chiral building block in the production of odorants.
- Research: Exploratory studies in organic synthesis and material science.
- Synthesis: The synthesis of such complex molecules often requires careful planning and execution, typically involving multiple steps including:
- Functional group transformation
- Chain lengthening through alkylation reactions
- Isomerization processes
- Chirality: The presence of chiral centers in this compound could lead to different stereoisomers, which might exhibit distinct biological activities. This property is crucial in the development of enantiomerically pure pharmaceuticals.
- Research Significance: Studying such compounds helps chemists understand the intricacies of molecular interactions, providing valuable insights into areas like enzyme catalysis and reaction mechanisms.
In conclusion, 8,8-dimethoxy-2,6-dimethyl-octan-2-ol stands as a testament to the complexities of organic chemistry, opening doors to various applications and research opportunities that continue to inspire chemists around the globe.
Synonyms
Hydroxycitronellal dimethyl acetal
8,8-Dimethoxy-2,6-dimethyloctan-2-ol
141-92-4
Laurine dimethyl acetal
8,8-Dimethoxy-2,6-dimethyl-2-octanol
Hydroxycitronellal DMA
2-Octanol, 8,8-dimethoxy-2,6-dimethyl-
1,1-Dimethoxy-3,7-dimethyl-7-octanol
FEMA No. 2585
OCTANAL, 7-HYDROXY-3,7-DIMETHYL-, DIMETHYL ACETAL
NSC 76412
Citronellal hydrate dimethylacetal
EINECS 205-510-9
7-Hydroxy-3,7-dimethyloctanal dimethyl acetal
DTXSID4047547
UNII-K989V651N4
AI3-05824
NSC-76412
K989V651N4
DTXCID2027547
Hydroxycitronella dimethyl acetal
7-Hydroxy-3,7-dimethyloctanal, dimethyl acetal
HYDROXYCITRONELLAL DIMETHYL ACETAL [FCC]
HYDROXYCITRONELLAL DIMETHYL ACETAL [FHFI]
(+/-)-HYDROXYCITRONELLAL DIMETHYL ACETAL
HYDROXYCITRONELLAL DIMETHYL ACETAL, (+/-)-
NCIOpen2_004111
SCHEMBL997419
7-Hydroxy-3, dimethyl acetal
hydroxycitronellal dimethylacetal
CHEMBL3184842
FEMA 2585
CHEBI:172458
NSC76412
Tox21_302540
Octanal,7-dimethyl-, dimethyl acetal
AKOS016011094
2-Octanol,8-dimethoxy-2,6-dimethyl-
Hydroxydihydrocitronellal dimethyl acetal
NCGC00256762-01
CAS-141-92-4
DB-360575
NS00012632
G84025
Hydroxycitronellal dimethyl acetal, >=95%, FCC
Q27282124
Solubility of 8,8-Dimethoxy-2,6-dimethyl-octan-2-ol
The solubility of 8,8-dimethoxy-2,6-dimethyl-octan-2-ol in various solvents can be quite intriguing due to its unique chemical structure. As an organic compound, its solubility characteristics exhibit some essential trends:
To summarize, the solubility behavior of 8,8-dimethoxy-2,6-dimethyl-octan-2-ol can be described as:
These solubility characteristics highlight the compound's potential applications and limitations in various chemical environments. Understanding these properties is crucial for determining its use in organic synthesis and formulation chemistry.