2,3,4-Trihydroxybenzaldehyde
2,3,4-Trihydroxybenzaldehyde structure
|
Common Name | 2,3,4-Trihydroxybenzaldehyde | ||
|---|---|---|---|---|
| CAS Number | 2144-08-3 | Molecular Weight | 154.120 | |
| Density | 1.6±0.1 g/cm3 | Boiling Point | 301.9±37.0 °C at 760 mmHg | |
| Molecular Formula | C7H6O4 | Melting Point | 159-161 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 150.6±23.0 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
|
Medicinal chemistry as a conduit for the modulation of quorum sensing.
J. Med. Chem. 53 , 7467-89, (2010)
|
|
|
Pyrogallol and its analogs can antagonize bacterial quorum sensing in Vibrio harveyi.
Bioorg. Med. Chem. Lett. 18 , 1567-72, (2008) Bacteria can coordinate community-wide behaviors through quorum sensing, that is, the secretion and sensing of autoinducer (AI) molecules. Bacterial quorum sensing is implicated in the regulation of pathologically relevant events such as biofilm formation, ba... |
|
|
Self-activating nuclease activity of copper (II) complexes of hydroxyl-rich ligands.
J. Inorg. Biochem. 100(1) , 51-7, (2006) Copper (II) complexes of Schiff bases derived from [1+1] condensation of salicylaldehyde, 2,3-dihydroxybenzaldehyde and 2,3,4-trihydroxybenzaldehyde with anthranilic acid (L1-L3) have been synthesized and characterized by elemental analyses, IR, UV-Vis spectr... |
|
|
Carbohydrazones of substituted salicylaldehydes as potential lead compounds for the development of narrow-spectrum antimicrobials.
Z. Naturforsch., C, J. Biosci. 62(7-8) , 483-6, (2007) Certain substituted salicylaldehydes are known to have highly potent antimicrobial activity against bacteria and fungi, but the mechanism underlying this remarkable activity is not known, and almost nothing has been reported on the effects of further modifica... |
|
|
1, 5-Dimethyl-2-phenyl-4-[(1E)-(2, 3, 4-trihydroxybenzylidene) amino]-1H-pyrazol-3 (2H)-one. Sun Y-F, et al.
Acta Crystallogr. Sect. E Struct. Rep. Online 63(5) , o2522-23, (2007)
|