Interesting facts
Exploring (3,5-Dimethylphenyl)methanol
(3,5-Dimethylphenyl)methanol, also known as a substituted benzyl alcohol, is a fascinating compound in the realm of organic chemistry. This compound holds significant interest due to its unique structural features and potential applications. Here are some compelling aspects:
- Structural Insights: The presence of two methyl groups on the phenyl ring at the 3 and 5 positions contributes to the compound's stability and influences its reactivity. This substitution pattern can affect the electronic distribution and sterics, making it a valuable subject for studying aromatic chemistry.
- Versatile Applications: Compounds like (3,5-dimethylphenyl)methanol are utilized in various fields, including:
- As intermediates in organic synthesis
- In the manufacture of fragrances and flavoring agents
- In pharmaceuticals due to potential biological activity
- Biological Activity: Research indicates that similar benzyl alcohol derivatives can exhibit noteworthy activities against certain organisms and have potential therapeutic effects, making (3,5-dimethylphenyl)methanol an interesting target for medicinal chemistry studies.
- Research Implications: The study of substitution effects in compounds such as (3,5-dimethylphenyl)methanol can provide insights into reaction mechanisms, such as electrophilic aromatic substitution and nucleophilic attacks, which are central concepts in organic chemistry.
In summary, (3,5-dimethylphenyl)methanol is not just a simple organic compound but a key player in the chemistry of substituted phenols. Its ability to serve as a building block in synthesizing more complex molecules highlights its importance in both academic research and industrial applications.
Synonyms
27129-87-9
3,5-DIMETHYLBENZYL ALCOHOL
Benzenemethanol, 3,5-dimethyl-
EINECS 248-241-2
DTXSID30181593
RefChem:487022
DTXCID70104084
248-241-2
(3,5-Dimethylphenyl)methanol
3,5-Dimethylbenzenemethanol
3,5-Dimethylbenzylalcohol
MFCD00004648
Benzyl alcohol, 3,5-dimethyl-
1-(Hydroxymethyl)-3,5-dimethylbenzene
(3,5-dimethylphenyl)methan-1-ol
Benzenemethanol,3,5-dimethyl-
7UXP4Z8EX9
SCHEMBL92965
3,5-Dimethyl benzyl alcohol
SCHEMBL396658
SCHEMBL6631552
SCHEMBL7784851
SCHEMBL10886772
(3,5-Dimethylphenyl)methanol #
CHEBI:231518
3,5-Dimethylbenzyl alcohol, 98%
BCP32520
3,5-Dimethyl-1-hydroxymethylbenzene
SBB064815
AKOS009157538
FD70768
AS-18666
SY009135
DB-067735
CS-0153260
NS00028258
ST51038048
EN300-1259109
F219220
3,5-Dimethylbenzenemethanol;3,5-Dimethylbenzylalcohol
InChI=1/C9H12O/c1-7-3-8(2)5-9(4-7)6-10/h3-5,10H,6H2,1-2H
Solubility of (3,5-dimethylphenyl)methanol
(3,5-dimethylphenyl)methanol, a compound characterized by its benzene ring with two methyl groups and a hydroxymethyl functional group, presents interesting solubility characteristics. Generally, the solubility of organic compounds in water can be influenced by factors such as molecular structure and functional groups.
In the case of (3,5-dimethylphenyl)methanol, the presence of the hydroxyl group (-OH) suggests that the compound has some degree of polar character, which tends to enhance its solubility in polar solvents like water. However, the two methyl groups contribute hydrophobic characteristics, potentially diminishing solubility. Therefore, its behavior in various solvents might be summarized as follows:
In conclusion, the solubility of (3,5-dimethylphenyl)methanol is a nuanced interplay of its molecular structure. As with many organic compounds, the balance between hydrophobic and hydrophilic characteristics ultimately dictates its solubility behavior in various solvents.