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
Targeted disruption of psbX and biochemical characterization of photosystem II complex in the thermophilic cyanobacterium Synechococcus elongatus.	2001 Feb	11230572
Catalysis of diaphorase reactions by Mycobacterium tuberculosis lipoamide dehydrogenase occurs at the EH4 level.	2003 Feb 25	12590611
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	12940734
Characterization of a new member of the flavoprotein disulfide reductase family of enzymes from Mycobacterium tuberculosis.	2004 Dec 10	15456792
1-Chloro-3,6-dimethoxy-2,5-dimethylbenzene and 1-chloro-3,6-dimethoxy-2,4-dimethylbenzene.	2004 Jul	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 Jun 16	15186175
2,6-dimethyl-1,4-benzoquinone 4-monooxime.	2005 Apr	15805639
Synthetic studies toward the kempane diterpenes. Construction of a key tricyclic intermediate.	2005 Oct 7	16172697
Synthesis of the tetracyclic core of the kempanes by a ring-closing metathesis strategy.	2006 Jan 5	16381591
Redox characteristics of a de novo quinone protein.	2007 Apr 5	17388486
Flavodiiron proteins in oxygenic photosynthetic organisms: photoprotection of photosystem II by Flv2 and Flv4 in Synechocystis sp. PCC 6803.	2009	19390625
Kinetics and mechanism of 2,6-dimethyl-aniline degradation by hydroxyl radicals.	2009 Dec 30	19692169
Quinone-enhanced reduction of nitric oxide by xanthine/xanthine oxidase.	2009 May	19301825
Chemical oxidation of 2,6-dimethylaniline in the fenton process.	2009 Nov 15	20028063
Chemical oxidation of 2,6-dimethylaniline by electrochemically generated Fenton's reagent.	2010 Apr 15	19963316
Role of quinones in the ascorbate reduction rates of S-nitrosoglutathione.	2010 Nov 15	20691779
Towards a systematic analysis of human short-chain dehydrogenases/reductases (SDR): Ligand identification and structure-activity relationships.	2015 Jun 5	25526675

Patents

Substance Class	Chemical Created by `admin` on `Sat Dec 16 00:09:45 GMT 2023` Edited by `admin` on `Sat Dec 16 00:09:45 GMT 2023`
Record UNII	HET5TF8ZGO
Record Status	`Validated (UNII)`
Record Version

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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