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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
Structure of 2,6-DIMETHYLBENZOQUINONE

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

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Targeted disruption of psbX and biochemical characterization of photosystem II complex in the thermophilic cyanobacterium Synechococcus elongatus.
2001 Feb
Catalysis of diaphorase reactions by Mycobacterium tuberculosis lipoamide dehydrogenase occurs at the EH4 level.
2003 Feb 25
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
Characterization of a new member of the flavoprotein disulfide reductase family of enzymes from Mycobacterium tuberculosis.
2004 Dec 10
1-Chloro-3,6-dimethoxy-2,5-dimethylbenzene and 1-chloro-3,6-dimethoxy-2,4-dimethylbenzene.
2004 Jul
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
Synthetic studies toward the kempane diterpenes. Construction of a key tricyclic intermediate.
2005 Oct 7
Kinetics and mechanism of 2,6-dimethyl-aniline degradation by hydroxyl radicals.
2009 Dec 30
Chemical oxidation of 2,6-dimethylaniline in the fenton process.
2009 Nov 15
Chemical oxidation of 2,6-dimethylaniline by electrochemically generated Fenton's reagent.
2010 Apr 15
Role of quinones in the ascorbate reduction rates of S-nitrosoglutathione.
2010 Nov 15
Towards a systematic analysis of human short-chain dehydrogenases/reductases (SDR): Ligand identification and structure-activity relationships.
2015 Jun 5
Patents
Name Type Language
2,6-DIMETHYLBENZOQUINONE
Systematic Name English
3,5-DIMETHYL-1,4-BENZOQUINONE
Systematic Name English
P-BENZOQUINONE, 2,6-DIMETHYL-
Common Name English
2,6-DIMETHYL-P-BENZOQUINONE
Common Name English
2,5-CYCLOHEXADIENE-1,4-DIONE, 2,6-DIMETHYL-
Systematic Name English
M-XYLOQUINONE
Common Name English
2,6-DIMETHYL-1,4-BENZOQUINONE
Systematic Name English
2,6-DIMETHYL-2,5-CYCLOHEXADIENE-1,4-DIONE
Systematic Name English
NSC-17549
Code English
3,5-DIMETHYLBENZOQUINONE
Systematic Name English
2,6-XYLOQUINONE
Common Name English
Code System Code Type Description
CAS
527-61-7
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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NSC
17549
Created by admin on Sat Dec 16 00:09:46 GMT 2023 , Edited by admin on Sat Dec 16 00:09:46 GMT 2023
PRIMARY
FDA UNII
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
PRIMARY
PUBCHEM
68241
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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EPA CompTox
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
PRIMARY
ECHA (EC/EINECS)
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
PRIMARY
MESH
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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