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About This Item
Linear Formula:
(CH3O)C6H3(OH)2
CAS Number:
Molecular Weight:
140.14
UNSPSC Code:
12162002
NACRES:
NA.23
PubChem Substance ID:
EC Number:
212-530-1
Beilstein/REAXYS Number:
2045285
MDL number:
Product Name
2-Methoxyhydroquinone, 98%
InChI key
LAQYHRQFABOIFD-UHFFFAOYSA-N
InChI
1S/C7H8O3/c1-10-7-4-5(8)2-3-6(7)9/h2-4,8-9H,1H3
SMILES string
COc1cc(O)ccc1O
assay
98%
form
solid
mp
88-91 °C (lit.)
Quality Level
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Related Categories
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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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
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
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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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