Interesting facts
Interesting Facts about 2,6-bis(hydroxymethyl)-4-methyl-phenol
2,6-bis(hydroxymethyl)-4-methyl-phenol is a fascinating compound that showcases a combination of molecular functionality and practical applications. Here are some key points to consider:
- Dual Functionality: This compound contains two hydroxymethyl groups which significantly enhance its reactivity and provide it with unique chemical properties that can be exploited in various synthesis processes.
- Phenolic Compound: As a phenol derivative, it exhibits characteristics similar to other phenolic compounds, offering strong antioxidant qualities. This makes it valuable in the preservation of various materials.
- Applications: It is primarily used in the production of adhesives and coatings, benefiting from its ability to improve durability and resistance to degradation.
- Research Potential: Due to its structural characteristics, 2,6-bis(hydroxymethyl)-4-methyl-phenol is of interest in the field of medicinal chemistry, where it can be studied for potential pharmaceutical applications.
- Environmental Impact: The use of such compounds in industrial applications raises questions about environmental sustainability, making it a subject for studies related to green chemistry and eco-friendly practices.
In summary, 2,6-bis(hydroxymethyl)-4-methyl-phenol is more than just a simple chemical compound; it represents a blend of chemistry and practical application that resonates through various fields, from industrial manufacture to research in medicinal chemistry. Its properties offer rich opportunities for innovation and exploration.
Synonyms
2,6-Bis(hydroxymethyl)-p-cresol
91-04-3
2,6-Bis(hydroxymethyl)-4-methylphenol
2,6-Dimethylol-p-cresol
(2-Hydroxy-5-methyl-1,3-phenylene)dimethanol
2-Hydroxy-5-methyl-1,3-benzenedimethanol
2,6-Dimethylol-4-methylphenol
1,3-BENZENEDIMETHANOL, 2-HYDROXY-5-METHYL-
2,6-Di(hydroxymethyl)-p-cresol
NSC 15838
3,5-Bis(hydroxymethyl)-p-cresol
alpha1,alpha,2-Trihydroxymesitylene
EINECS 202-036-4
BRN 1240237
Q99HT08S5N
DML-PC
.alpha.1,.alpha.3-Mesitylenediol, 2-hydroxy-
NSC-15838
26DMPC
alpha(sup 1),alpha(sup 3),2-Trihydroxymesitylene
alpha1,alpha3-Mesitylenediol, 2-hydroxy-
DTXSID2059017
4-06-00-07411 (Beilstein Handbook Reference)
MFCD00004619
.alpha.1,.alpha.3,2-Trihydroxymesitylene
2,6-Di(hydroxymethyl)-4-methylphenol
2,6-bis-(hydroxymethyl)-p-cresol
NSC15838
4-Methyl-2,6-bis(hydroxymethyl)-phenol
.alpha.1, 2-hydroxy-
1, 2-hydroxy-5-methyl-
UNII-Q99HT08S5N
Oprea1_724006
Oprea1_756581
SCHEMBL187792
DTXCID6048709
.alpha.1,2-Trihydroxymesitylene
2,6-Bis(hydroxymethyl)-p-kresol
2,6-Bis(hydroxylmethyl)-p-cresol
KUC106807N
2,6-bis(hydroxy-methyl)-p-cresol
alpha1,alpha3,2-Trihydroxymesitylene
STK394976
AKOS000268430
2,6-Bis-hydroxymethyl-4-methyl-phenol
FB34747
PS-4205
SB83890
2,6-Bis(hydroxymethyl)-p-cresol, 95%
KSC-11-237-11
.alpha.1,.alpha.3, 2-Trihydroxymesitylene
DB-010995
B1525
CS-0204260
NS00020357
D88821
alpha1,alpha3-Mesitylenediol, 2-hydroxy-(8CI)
AE-562/40177794
Q27287141
alpha(sup 1),alpha(sup 3)-Mesitylenediol, 2-hydroxy-
F1244-0104
alpha(sup 1),alpha(sup 3)-Mesitylenediol, 2-hydroxy-(7CI,8CI)
Solubility of 2,6-bis(hydroxymethyl)-4-methyl-phenol
The solubility of 2,6-bis(hydroxymethyl)-4-methyl-phenol can be quite intriguing due to its unique molecular structure. This compound, characterized by multiple hydroxymethyl groups, tends to exhibit the following solubility attributes:
In summary, 2,6-bis(hydroxymethyl)-4-methyl-phenol demonstrates preferential solubility in polar solvents, enabling its use in various chemical applications where solubility and reactivity in such environments are pivotal.