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 |
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Targeted disruption of psbX and biochemical characterization of photosystem II complex in the thermophilic cyanobacterium Synechococcus elongatus. | 2001 Feb |
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Catalysis of diaphorase reactions by Mycobacterium tuberculosis lipoamide dehydrogenase occurs at the EH4 level. | 2003 Feb 25 |
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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 Sep 3 |
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Characterization of a new member of the flavoprotein disulfide reductase family of enzymes from Mycobacterium tuberculosis. | 2004 Dec 10 |
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1-Chloro-3,6-dimethoxy-2,5-dimethylbenzene and 1-chloro-3,6-dimethoxy-2,4-dimethylbenzene. | 2004 Jul |
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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 Jun 16 |
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Synthetic studies toward the kempane diterpenes. Construction of a key tricyclic intermediate. | 2005 Oct 7 |
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Kinetics and mechanism of 2,6-dimethyl-aniline degradation by hydroxyl radicals. | 2009 Dec 30 |
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Chemical oxidation of 2,6-dimethylaniline in the fenton process. | 2009 Nov 15 |
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Chemical oxidation of 2,6-dimethylaniline by electrochemically generated Fenton's reagent. | 2010 Apr 15 |
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Role of quinones in the ascorbate reduction rates of S-nitrosoglutathione. | 2010 Nov 15 |
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Towards a systematic analysis of human short-chain dehydrogenases/reductases (SDR): Ligand identification and structure-activity relationships. | 2015 Jun 5 |
Patents
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527-61-7
Created by
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17549
Created by
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HET5TF8ZGO
Created by
admin on Sat Dec 16 00:09:46 GMT 2023 , Edited by admin on Sat Dec 16 00:09:46 GMT 2023
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68241
Created by
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DTXSID00200664
Created by
admin on Sat Dec 16 00:09:46 GMT 2023 , Edited by admin on Sat Dec 16 00:09:46 GMT 2023
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208-420-8
Created by
admin on Sat Dec 16 00:09:46 GMT 2023 , Edited by admin on Sat Dec 16 00:09:46 GMT 2023
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C035577
Created by
admin on Sat Dec 16 00:09:46 GMT 2023 , Edited by admin on Sat Dec 16 00:09:46 GMT 2023
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SUBSTANCE RECORD