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assay
98%
form
solid
mp
134-137 °C (lit.)
solubility
acetone: 0.25 g/10 mL, clear, colorless to deep brown-yellow
SMILES string
OC(c1ccco1)C(=O)c2ccco2
InChI
1S/C10H8O4/c11-9(7-3-1-5-13-7)10(12)8-4-2-6-14-8/h1-6,9,11H
InChI key
MIJRFWVFNKQQDK-UHFFFAOYSA-N
Gene Information
human ... ACHE(43) , BCHE(590) , CES1(1066)
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Application
Furoin was used as fluorogenic reagent for the selective and sensitive liquid chromatographic determination of various guanidines.
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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Origins of life and evolution of the biosphere : the journal of the International Society for the Study of the Origin of Life, 49(4), 199-211 (2019-12-10)
The chemistry of imidazolium-catalyzed imidazolium synthesis was studied as part of an effort to develop a plausible prebiotic synthesis of a small catalytic molecule capable of catalyzing its own synthesis. Specifically, we investigated the one-pot 1-ethyl-3-methylimidazolium acetate (EMIM-Ac) catalyzed synthesis
Analytica chimica acta, 999, 169-175 (2017-12-20)
Porous organic molecular cages, as a new type of porous materials, have in recent years attracted a tremendous amount of attention for their potential applications. However, to the best of our knowledge, there has been no attempt to utilize porous
Journal of pharmaceutical and biomedical analysis, 48(3), 754-759 (2008-09-27)
Furoin, a benzoin analogue, was examined as novel fluorogenic reagent for the selective and sensitive LC determination of various guanidines after pre-column derivatization. The derivatization reaction was carried out at 100 degrees C for 5 min to give adducts that
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