Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C9H12O2 |
| Molecular Weight | 152.1904 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=CC(O)=C(C)C(C)=C1O
InChI
InChIKey=AUFZRCJENRSRLY-UHFFFAOYSA-N
InChI=1S/C9H12O2/c1-5-4-8(10)6(2)7(3)9(5)11/h4,10-11H,1-3H3
| Molecular Formula | C9H12O2 |
| Molecular Weight | 152.1904 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Trimethylhydroquinone (2,3,5-Trimethylhydroquinone, TMHQ) is a compound with a wide range of important practical applications. As shown by data from the patent literature, this compound can be used in the synthesis of dyes, pigments, antioxidants, polymerization inhibitors, and other important chemicals. However, the main use of this compound is as an intermediate in the industrial synthesis of vitamin E. Because of the importance of vitamin E in medicine, food manufacturing, and cattle breeding, there is continuing interest in the methods for the preparation of 2,3,5-trimethylhydroquinone. Trimethylhydroquinone presented obvious in vitro anti-MRSA activity.
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Trimethylsilyl pentafluorophenylbis(trifluoromethanesulfonyl)methide as a super Lewis acid catalyst for the condensation of trimethylhydroquinone with isophytol. | 2003-12-01 |
|
| [Inhibition of peroxidase oxidation of aromatic amines by substituted phenols]. | 2003-10-03 |
|
| A short synthesis of troglitazone: an antidiabetic drug for treating insulin resistance. | 1999-12-20 |
Patents
| Substance Class |
Chemical
Created
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Mon Mar 31 19:09:39 GMT 2025
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GSY6340N4A
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