Home Other Building Blocks 2,6-Dimethylbenzoquinone

2,6-Dimethylbenzoquinone

CAS No.:
527-61-7
Catalog Number:
AG003G5M
Molecular Formula:
C8H8O2
Molecular Weight:
136.1479
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
>98.0%(GC)
1 week
United States
$78
- +
5g
>98.0%(GC)
1 week
United States
$178
- +
25g
>98.0%(GC)
1 week
United States
$527
- +
Product Description
Catalog Number:
AG003G5M
Chemical Name:
2,6-Dimethylbenzoquinone
CAS Number:
527-61-7
Molecular Formula:
C8H8O2
Molecular Weight:
136.1479
MDL Number:
MFCD00001605
IUPAC Name:
2,6-dimethylcyclohexa-2,5-diene-1,4-dione
InChI:
InChI=1S/C8H8O2/c1-5-3-7(9)4-6(2)8(5)10/h3-4H,1-2H3
InChI Key:
SENUUPBBLQWHMF-UHFFFAOYSA-N
SMILES:
O=C1C=C(C)C(=O)C(=C1)C
EC Number:
208-420-8
UNII:
HET5TF8ZGO
NSC Number:
17549
Properties
Complexity:
232  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
136.052g/mol
Formal Charge:
0
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
136.15g/mol
Monoisotopic Mass:
136.052g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
34.1A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.2  
Literature
Title Journal
Towards a systematic analysis of human short-chain dehydrogenases/reductases (SDR): Ligand identification and structure-activity relationships. Chemico-biological interactions 20150605
The pea SAD short-chain dehydrogenase/reductase: quinone reduction, tissue distribution, and heterologous expression. Plant physiology 20110401
Role of quinones in the ascorbate reduction rates of S-nitrosoglutathione. Free radical biology & medicine 20101115
Photolabile ubiquinone analogues for identification and characterization of quinone binding sites in proteins. Bioorganic & medicinal chemistry 20100515
Chemical oxidation of 2,6-dimethylaniline by electrochemically generated Fenton's reagent. Journal of hazardous materials 20100415
Kinetics and mechanism of 2,6-dimethyl-aniline degradation by hydroxyl radicals. Journal of hazardous materials 20091230
Chemical oxidation of 2,6-dimethylaniline in the fenton process. Environmental science & technology 20091115
Quinone-enhanced reduction of nitric oxide by xanthine/xanthine oxidase. Chemical research in toxicology 20090501
Flavodiiron proteins in oxygenic photosynthetic organisms: photoprotection of photosystem II by Flv2 and Flv4 in Synechocystis sp. PCC 6803. PloS one 20090101
Redox characteristics of a de novo quinone protein. The journal of physical chemistry. B 20070405
Synthesis of the tetracyclic core of the kempanes by a ring-closing metathesis strategy. Organic letters 20060105
Synthetic studies toward the kempane diterpenes. Construction of a key tricyclic intermediate. Organic & biomolecular chemistry 20051007
2,6-dimethyl-1,4-benzoquinone 4-monooxime. Acta crystallographica. Section C, Crystal structure communications 20050401
Characterization of a new member of the flavoprotein disulfide reductase family of enzymes from Mycobacterium tuberculosis. The Journal of biological chemistry 20041210
1-Chloro-3,6-dimethoxy-2,5-dimethylbenzene and 1-chloro-3,6-dimethoxy-2,4-dimethylbenzene. Acta crystallographica. Section C, Crystal structure communications 20040701
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. Journal of the American Chemical Society 20040616
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. Journal of the American Chemical Society 20030903
Catalysis of diaphorase reactions by Mycobacterium tuberculosis lipoamide dehydrogenase occurs at the EH4 level. Biochemistry 20030225
Targeted disruption of psbX and biochemical characterization of photosystem II complex in the thermophilic cyanobacterium Synechococcus elongatus. Plant & cell physiology 20010201
Properties