Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C8H8O2 |
| Molecular Weight | 136.1479 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=CC(=O)C=C(C)C1=O
InChI
InChIKey=SENUUPBBLQWHMF-UHFFFAOYSA-N
InChI=1S/C8H8O2/c1-5-3-7(9)4-6(2)8(5)10/h3-4H,1-2H3
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Towards a systematic analysis of human short-chain dehydrogenases/reductases (SDR): Ligand identification and structure-activity relationships. | 2015-06-05 |
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| Role of quinones in the ascorbate reduction rates of S-nitrosoglutathione. | 2010-11-15 |
|
| Chemical oxidation of 2,6-dimethylaniline by electrochemically generated Fenton's reagent. | 2010-04-15 |
|
| Kinetics and mechanism of 2,6-dimethyl-aniline degradation by hydroxyl radicals. | 2009-12-30 |
|
| Chemical oxidation of 2,6-dimethylaniline in the fenton process. | 2009-11-15 |
|
| Quinone-enhanced reduction of nitric oxide by xanthine/xanthine oxidase. | 2009-05 |
|
| Flavodiiron proteins in oxygenic photosynthetic organisms: photoprotection of photosystem II by Flv2 and Flv4 in Synechocystis sp. PCC 6803. | 2009 |
|
| Redox characteristics of a de novo quinone protein. | 2007-04-05 |
|
| Synthesis of the tetracyclic core of the kempanes by a ring-closing metathesis strategy. | 2006-01-05 |
|
| Synthetic studies toward the kempane diterpenes. Construction of a key tricyclic intermediate. | 2005-10-07 |
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| 2,6-dimethyl-1,4-benzoquinone 4-monooxime. | 2005-04 |
|
| Characterization of a new member of the flavoprotein disulfide reductase family of enzymes from Mycobacterium tuberculosis. | 2004-12-10 |
|
| 1-Chloro-3,6-dimethoxy-2,5-dimethylbenzene and 1-chloro-3,6-dimethoxy-2,4-dimethylbenzene. | 2004-07 |
|
| Efficient methods for the preparation of alkyl-aryl and symmetrical or unsymmetrical dialkyl ethers between alcohols and phenols or two alcohols by oxidation-reduction condensation. | 2004-06-16 |
|
| A convenient method for the preparation of inverted tert-alkyl carboxylates from chiral tert-alcohols by a new type of oxidation-reduction condensation using 2,6-dimethyl-1,4-benzoquinone. | 2003-09-03 |
|
| Catalysis of diaphorase reactions by Mycobacterium tuberculosis lipoamide dehydrogenase occurs at the EH4 level. | 2003-02-25 |
|
| Targeted disruption of psbX and biochemical characterization of photosystem II complex in the thermophilic cyanobacterium Synechococcus elongatus. | 2001-02 |
Patents
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| Code System | Code | Type | Description | ||
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527-61-7
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17549
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HET5TF8ZGO
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68241
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DTXSID00200664
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208-420-8
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C035577
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SUBSTANCE RECORD
