2,5-Dihydroxybenzaldehyde
2,5-Dihydroxybenzaldehyde structure
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Common Name | 2,5-Dihydroxybenzaldehyde | ||
|---|---|---|---|---|
| CAS Number | 1194-98-5 | Molecular Weight | 138.121 | |
| Density | 1.4±0.1 g/cm3 | Boiling Point | 276.1±20.0 °C at 760 mmHg | |
| Molecular Formula | C7H6O3 | Melting Point | 97-99 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 135.1±18.3 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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Liquid chromatographic/electrospray ionization mass spectrometric identification of the oxidation end-products of trans-resveratrol in aqueous solutions.
Rapid Commun. Mass Spectrom. 24(5) , 634-42, (2010) trans-Resveratrol (3,5,4'-trihydroxystilbene) is a natural polyphenolic compound that exhibits antioxidant properties. Our study aimed at studying the HO*-induced oxidation of resveratrol (100 micromol.L(-1)) in aerated aqueous solutions. Gamma radiolysis of ... |
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A bioanode based on MWCNT/protein-assisted co-immobilization of glucose oxidase and 2,5-dihydroxybenzaldehyde for glucose fuel cells.
Biosens. Bioelectron. 25(11) , 2515-21, (2010) This paper describes an easy-to-prepare, robust bioanode constructed on a polyester-supported screen-printed carbon paste electrode (SPCE) for glucose biofuel cells. To prepare the bioanode, carboxylated multi-walled carbon nanotubes (MWCNTs) were drop-coated... |
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The reductive half-reaction of xanthine oxidase. Reaction with aldehyde substrates and identification of the catalytically labile oxygen.
J. Biol. Chem. 274(6) , 3323-30, (1999) The kinetics of xanthine oxidase has been investigated with the aim of addressing several outstanding questions concerning the reaction mechanism of the enzyme. Steady-state and rapid kinetic studies with the substrate 2,5-dihydroxybenzaldehyde demonstrated t... |
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Sequential C-N and C-O bond formation in a single pot: synthesis of 2H-benzo[b][1,4]oxazines from 2,5-dihydroxybenzaldehyde and amino acid precursors.
Org. Lett. 14(2) , 552-5, (2012) Functionalized β-aryl alanine ester derivatives were found to undergo rapid C-N and C-O bond formation with quinol carbonyl compounds to afford 2H-benzo[b][1,4]oxazines in good to excellent yields. This unprecedented finding reported herein offers a straightf... |
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Analysis of aliphatic amines in air samples by HPLC with electrochemical detection.
J. Pharm. Biomed. Anal. 29(6) , 1105-11, (2002) A method was developed for the analysis of primary aliphatic amines by high performance liquid chromatography coupled with electrochemical detector. The electrochemical oxidation of aliphatic amines derivatized with 2,5-dihydroxybenzaldehyde was investigated ... |
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Validation of malondialdehyde and 4-hydroxy-2-trans-nonenal measurement in plasma by NICI-GC-MS.
J. Biochem. 123(5) , 918-23, (1998) Measurement of the concentrations of aldehydes in biological samples has become the object of much effort due to their relevance in relation to the toxic effects of lipid peroxidation, through which a number of aldehydes are derived. We have reconsidered a pr... |
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Diffusion-free mediator based miniature biofuel cell anode fabricated on a carbon-MEMS electrode.
Langmuir 28(39) , 14055-64, (2012) We report on the functionalization of a micropatterned carbon electrode fabricated using the carbon-MEMS process for its use as a miniature diffusion-free glucose oxidase anode. Carbon-MEMS based electrodes offer precise manufacturing control on both the micr... |
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Synthesis and in vitro antiproliferative activity of new phenylaminoisoquinolinequinones against cancer cell lines.
Molecules 18(1) , 721-34, (2013) A variety of phenylaminoisoquinolinequinones were synthesized and tested for their antiproliferative activity against three human-tumor derived cancer cell lines. The new aminoquinones were prepared from 4-methoxycarbonyl-3-methylisoquinoline-5,8-quinone (1) ... |