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Dokumente

176893

Sigma-Aldrich

2-Methoxyhydrochinon

98%

Synonym(e):

2,5-Dihydroxy-anisol

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About This Item

Lineare Formel:
(CH3O)C6H3(OH)2
CAS-Nummer:
824-46-4
Molekulargewicht:
140.14
Beilstein:
2045285
EG-Nummer:
212-530-1
MDL-Nummer:
MFCD00013971
UNSPSC-Code:
12162002
PubChem Substanz-ID:
24850606
NACRES:
NA.23

Assay

98%

Form

solid

mp (Schmelzpunkt)

88-91 °C (lit.)

SMILES String

COc1cc(O)ccc1O

InChI

1S/C7H8O3/c1-10-7-4-5(8)2-3-6(7)9/h2-4,8-9H,1H3

InChIKey

LAQYHRQFABOIFD-UHFFFAOYSA-N

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Verwandte Kategorien

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

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David Sillam-Dussès et al.
PloS one, 7(10), e46431-e46431 (2012-10-17)
Labial glands are present in all castes and developmental stages of all termite species. In workers, their secretion contains a food-marking pheromone and digestive enzymes, while soldier secretion plays a defensive role. However, these functions were studied only in a
Koorosh Ashrafi et al.
International journal of pharmaceutics, 524(1-2), 226-237 (2017-04-05)
Drug release from chemoembolization microspheres stimulated by the presence of a chemically reducing environment may provide benefits for targeting drug resistant and metastatic hypoxic tumours. A water-soluble disulfide-based bifunctional cross-linker bis(acryloyl)-(l)-cystine (BALC) was synthesised, characterised and incorporated into a modified
Shou Ito et al.
Biotechnology for biofuels, 13, 18-18 (2020-02-06)
Vanillin is the main byproduct of alkaline-pretreated lignocellulosic biomass during the process of fermentable-sugar production and a potent inhibitor of ethanol production by yeast. Yeast cells are usually exposed to vanillin during the industrial production of bioethanol from lignocellulosic biomass.
Maher A Qaddoura et al.
International journal of molecular sciences, 10(11), 4772-4788 (2010-01-21)
Several divinylic mesogenic monomers were synthesized based on coupling the monomer 4-(4-pentenyloxy)benzoic acid with chlorohydroquinone, 2,5-dihydroxy- acetophenone, methylhydroquinone or 2-methoxyhydroquinone. This resulted in novel mesogens of phenylene esters with different lateral substituent groups. The effect of the lateral substituent group
Denilson F Oliveira et al.
Experimental parasitology, 199, 17-23 (2019-02-23)
Exposing second-stage juveniles (J2) of Meloidogyne incognita in vitro to a phenolic compound sometimes fails to cause J2 mortality, but in tests in vivo the same compound may reduce the infectivity and population of the nematode. This work aimed to

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