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Key Documents

192651

Sigma-Aldrich

Furoin

98%

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About This Item

Empirical Formula (Hill Notation):
C10H8O4
CAS Number:
Molecular Weight:
192.17
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

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

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Application

Furoin was used as fluorogenic reagent for the selective and sensitive liquid chromatographic determination of various guanidines.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Arthur L Weber et al.
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
Jun-Hui Zhang et al.
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
R Gatti et al.
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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