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Merck

D149705

Sigma-Aldrich

2,6-Dimethylbenzoquinone

99%

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About This Item

Fórmula lineal:
(CH3)2C6H2-1,4-(=O)2
Número de CAS:
Peso molecular:
136.15
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

99%

form

solid

mp

71-73 °C (lit.)

SMILES string

CC1=CC(=O)C=C(C)C1=O

InChI

1S/C8H8O2/c1-5-3-7(9)4-6(2)8(5)10/h3-4H,1-2H3

InChI key

SENUUPBBLQWHMF-UHFFFAOYSA-N

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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A C Stewart
The Biochemical journal, 204(3), 705-712 (1982-06-15)
1. Photosynthetic electron transport from water to lipophilic Photosystem II acceptors was stimulated 3--5-fold by high concentrations (greater than or equal to 1 M) of salts containing anions such as citrate, succinate and phosphate that are high in the Hofmeister
Mustafa Odabaşoğlu et al.
Acta crystallographica. Section C, Crystal structure communications, 61(Pt 4), o240-o242 (2005-04-05)
Molecules of the title compound, C8H9NO2, are linked into sheets by a combination of C-H...N, O-H...N and O-H...O hydrogen bonds and C-H...pi interactions. The hydrogen bonds are arranged as described by the graph-set ring notations R(2)(2)(7) and R(3)(3)(5), and a
Argyrides Argyrou et al.
Biochemistry, 42(7), 2218-2228 (2003-02-20)
Lipoamide dehydrogenase catalyzes the reversible NAD(+)-dependent oxidation of the dihydrolipoyl cofactors that are covalently attached to the acyltransferase components of the pyruvate dehydrogenase, alpha-ketoglutarate dehydrogenase, and glycine reductase multienzyme complexes. It contains two redox centers: a tightly, but noncovalently, bound
Sam Hay et al.
The journal of physical chemistry. B, 111(13), 3488-3495 (2007-03-29)
The electrochemistry of 2,6-dimethylbenzoquinone (DMBQ) has been characterized for three different systems: DMBQ freely solvated in aqueous buffer; DMBQ bound to a neutral, blocked cysteine (N-acetyl-L-cysteine methyl ester) and the resulting DMBQ-bCys compound solvated in aqueous buffer; and DMBQ bound
D Kim et al.
Chemistry & biology, 5(2), 103-117 (1998-03-13)
The temporal and spatial control of the transition from vegetative to parasitic growth is critical to any parasite, but is essential to the sessile parasitic plants. It has been proposed that this transition in Striga spp. is controlled simply by

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