Interesting facts
Interesting Facts about 4-(Hydroxymethyl)-2,6-dimethoxy-phenol
4-(Hydroxymethyl)-2,6-dimethoxy-phenol, often recognized in the realm of organic chemistry for its aromatic properties, is a fascinating compound with various applications. Here are some engaging facts about this compound:
- Chemical Structure: This compound belongs to the class of phenolic compounds, characterized by a hydroxymethyl group and two methoxy groups attached to the aromatic ring. Such substitutions can significantly alter the chemical reactivity and properties of the base phenol structure.
- Natural Occurrence: Compounds with similar structures are often found in natural sources. In particular, they can be derived from certain plants and are known to exhibit antioxidant properties, which makes them valuable in both health and cosmetic applications.
- Biological Activity: Research indicates that this compound has potential biological activities, including antimicrobial and anti-inflammatory effects. Its structure allows it to interact with biological systems effectively, which is promising for pharmaceutical development.
- Applications:
- In the field of cosmetics, it can be utilized for its skin-soothing properties.
- As an ingredient in personal care products due to its desirable scent and potential benefits for skin health.
- Research and Development: Ongoing studies focus on the synthesis and modification of this compound to enhance its efficacy and reduce potential side effects in therapeutic applications. This highlights the dynamic nature of compound research!
- Environmental Relevance: The presence of phenolic compounds like 4-(Hydroxymethyl)-2,6-dimethoxy-phenol in the environment often raises discussions about their biodegradability and impact on ecosystems, prompting studies on their fate in nature.
- Quote from Chemistry: "The beauty of chemistry lies in its ability to turn simple compounds into complex functionalities." This compound is a testament to that beauty.
In summary, 4-(Hydroxymethyl)-2,6-dimethoxy-phenol is more than just a name; it embodies a world of chemical wonders, highlighting the intricate balance between structure and function at the molecular level.
Synonyms
530-56-3
4-HYDROXY-3,5-DIMETHOXYBENZYL ALCOHOL
Syringyl alcohol
syringic alcohol
3,5-Dimethoxy-4-hydroxybenzyl alcohol
Benzenemethanol, 4-hydroxy-3,5-dimethoxy-
2,6-dimethoxy-4-(hydroxymethyl)phenol
K7G66I59XC
EINECS 208-485-2
CHEBI:86948
DTXSID00201050
3,5-dimethoxy-4-hydroxy-benzylalcohol
4-HYDROXY-3,5-DIMETHOXYBENZENEMETHANOL
DTXCID00123541
208-485-2
4-(Hydroxymethyl)-2,6-dimethoxyphenol
UNII-K7G66I59XC
4-Hydroxy-3,5-dimethoxybenzylalcohol
MFCD00016871
SBB058585
bmse010007
SCHEMBL1067240
HY-N6654
s4942
AKOS009159361
CCG-266464
FD71202
4-(hydroxymethyl)-2,6-dimethoxy-phenol
AS-81451
4-(Hydroxymethyl)-2,6-dimethoxyphenol #
DB-052244
CS-0083210
NS00022304
G12063
EN300-1837509
Q2376479
InChI=1/C9H12O4/c1-12-7-3-6(5-10)4-8(13-2)9(7)11/h3-4,10-11H,5H2,1-2H
Solubility of 4-(hydroxymethyl)-2,6-dimethoxy-phenol
The solubility of 4-(hydroxymethyl)-2,6-dimethoxy-phenol can be influenced by several factors, including temperature, solvent type, and the compound's structure. Here are some key points regarding its solubility:
In general, the solubility of organic compounds like 4-(hydroxymethyl)-2,6-dimethoxy-phenol can be summarized with the phrase: "Like dissolves like." Therefore, this compound is expected to be more soluble in organic solvents compared to water. However, specific solubility values and behaviors can be determined only through experimental evaluations.