2,6-DIMETHYLBENZOQUINONE

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 Search

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

Molecular Formula	C8H8O2
Molecular Weight	136.1479
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

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	25526675
Role of quinones in the ascorbate reduction rates of S-nitrosoglutathione.	2010-11-15	20691779
Chemical oxidation of 2,6-dimethylaniline by electrochemically generated Fenton's reagent.	2010-04-15	19963316
Kinetics and mechanism of 2,6-dimethyl-aniline degradation by hydroxyl radicals.	2009-12-30	19692169
Chemical oxidation of 2,6-dimethylaniline in the fenton process.	2009-11-15	20028063
Quinone-enhanced reduction of nitric oxide by xanthine/xanthine oxidase.	2009-05	19301825
Flavodiiron proteins in oxygenic photosynthetic organisms: photoprotection of photosystem II by Flv2 and Flv4 in Synechocystis sp. PCC 6803.	2009	19390625
Redox characteristics of a de novo quinone protein.	2007-04-05	17388486
Synthesis of the tetracyclic core of the kempanes by a ring-closing metathesis strategy.	2006-01-05	16381591
Synthetic studies toward the kempane diterpenes. Construction of a key tricyclic intermediate.	2005-10-07	16172697
2,6-dimethyl-1,4-benzoquinone 4-monooxime.	2005-04	15805639
Characterization of a new member of the flavoprotein disulfide reductase family of enzymes from Mycobacterium tuberculosis.	2004-12-10	15456792
1-Chloro-3,6-dimethoxy-2,5-dimethylbenzene and 1-chloro-3,6-dimethoxy-2,4-dimethylbenzene.	2004-07	15237190
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	15186175
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	12940734
Catalysis of diaphorase reactions by Mycobacterium tuberculosis lipoamide dehydrogenase occurs at the EH4 level.	2003-02-25	12590611
Targeted disruption of psbX and biochemical characterization of photosystem II complex in the thermophilic cyanobacterium Synechococcus elongatus.	2001-02	11230572

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 20:32:20 GMT 2025` Edited by `admin` on `Mon Mar 31 20:32:20 GMT 2025`
Record UNII	HET5TF8ZGO
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

2,6-DIMETHYLBENZOQUINONE

Systematic Name

English

NSC-17549

Preferred 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

3,5-DIMETHYLBENZOQUINONE

Systematic Name

English

2,6-XYLOQUINONE

Common Name

English

Code System Code Type Description

CAS

527-61-7