Interesting facts
Interesting Facts about 3-methyl-4-methylsulfanyl-phenol
3-methyl-4-methylsulfanyl-phenol, often referred to in the realm of organic chemistry as a compound featuring both methyl and methylsulfanyl groups, presents several captivating aspects:
- Structure and Stability: The presence of both methyl and methylsulfanyl groups influences the compound's reactivity and stability. These functional groups can aid in the stabilization of the phenolic structure, contributing to its unique chemical behavior.
- Applications in Synthesis: This compound can serve as a versatile intermediate in organic synthesis. Its functional groups may be essential for synthesizing more complex molecules, making it valuable in research and industrial applications.
- Biological Importance: Compounds like 3-methyl-4-methylsulfanyl-phenol often exhibit interesting biological activity. Related phenolic compounds have been studied for their potential antioxidant properties, which may contribute to health benefits in various contexts.
- Flavor and Fragrance: Methylsulfanyl phenols might appear in natural products, leading to potential use in flavoring and fragrance applications where sulfur-containing compounds can impart desired scents or tastes.
- Chemical Properties: The arrangement of substituents around the phenolic ring can significantly influence the compound's acidity, affecting its reactivity in various chemical reactions. Understanding these properties is crucial for chemists working on new reactions or developing new materials.
In summary, 3-methyl-4-methylsulfanyl-phenol is not just a simple compound; its structure and functional groups open the door to exciting possibilities in chemical synthesis, biological studies, and industrial applications. As with many compounds in organic chemistry, the exploration of its properties may lead to novel discoveries and innovations.
Synonyms
3-Methyl-4-(methylthio)phenol
3120-74-9
4-(Methylthio)-m-cresol
Methylthiomethylphenol
Phenol, 3-methyl-4-(methylthio)-
USAF MA-17
4-(Methylthio)-3-methylphenol
m-CRESOL, 4-(METHYLTHIO)-
NSC 87560
EINECS 221-496-7
BRN 1210322
DTXSID0051996
AI3-28074
304RF69F8F
NSC-87560
DTXCID3030559
EC 221-496-7
3-06-00-04504 (Beilstein Handbook Reference)
221-496-7
MMTP
3-methyl-4-methylsulfanylphenol
3-Methyl-4-(1-methylthio)phenol
3-Methyl-4-(methylsulfanyl)phenol
4-(methylsulfanyl)-m-cresol
p-Methylthio-m-methylphenol
UNII-304RF69F8F
MFCD00045773
4-Methylthio-meta-cresol
WLN: QR C1 DS1
SCHEMBL1128366
3-methyl-4-methylmercaptophenol
4-methylmercapto-3-methylphenol
CHEMBL3560322
CHEBI:38681
4-methylsulfanyl-3-methyl-phenol
NSC87560
Tox21_303747
CCG-40509
3-Methyl-4-(methylsulfanyl)phenol #
AKOS003609815
3-Methyl-4-(methylthio)phenol, 97%
AC-8743
AT20905
NCGC00357052-01
AS-12573
CAS-3120-74-9
DB-047985
CS-0173482
M0531
NS00004503
EN300-125328
Q27117942
Z277164168
InChI=1/C8H10OS/c1-6-5-7(9)3-4-8(6)10-2/h3-5,9H,1-2H
Solubility of 3-methyl-4-methylsulfanyl-phenol
3-methyl-4-methylsulfanyl-phenol, often referred to in the context of its solubility properties, exhibits interesting behavior in various solvents. The solubility of this compound can be influenced by various factors such as temperature, the presence of other solutes, and the nature of the solvent.
Solubility Characteristics
It is essential to note that the presence of the -SH group introduces polarity, which is favorable for solubility in polar environments. In contrast, the presence of bulky methyl groups may hinder accessibility to certain solvent molecules, potentially decreasing solubility in some cases. Understanding these solubility dynamics is crucial for applications involving 3-methyl-4-methylsulfanyl-phenol, as they significantly impact its reactivity and behavior in chemical processes.