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D149705

Sigma-Aldrich

2,6-Dimethylbenzoquinone

99%

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About This Item

Fórmula linear:
(CH3)2C6H2-1,4-(=O)2
Número CAS:
Peso molecular:
136.15
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22

Nível de qualidade

Ensaio

99%

Formulário

solid

pf

71-73 °C (lit.)

cadeia de caracteres SMILES

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

chave InChI

SENUUPBBLQWHMF-UHFFFAOYSA-N

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)


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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
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
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

Global Trade Item Number

SKUGTIN
D149705-1G4061825590455
D149705-50G
D149705-5G4061831835694

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