2,4-dimethoxybenzaldehyde
2,4-dimethoxybenzaldehyde structure
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Common Name | 2,4-dimethoxybenzaldehyde | ||
|---|---|---|---|---|
| CAS Number | 613-45-6 | Molecular Weight | 166.174 | |
| Density | 1.1±0.1 g/cm3 | Boiling Point | 307.8±0.0 °C at 760 mmHg | |
| Molecular Formula | C9H10O3 | Melting Point | 67-69 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 124.7±8.2 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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Antifungal activity of redox-active benzaldehydes that target cellular antioxidation.
Ann. Clin. Microbiol. Antimicrob. 10 , 23, (2011) Disruption of cellular antioxidation systems should be an effective method for control of fungal pathogens. Such disruption can be achieved with redox-active compounds. Natural phenolic compounds can serve as potent redox cyclers that inhibit microbial growth... |
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Rational design of inhibitors of VirA-VirG two-component signal transduction.
Bioorg. Med. Chem. Lett. 17 , 3281-6, (2007) VirA-VirG two-component system regulates the vir (virulence) operon in response to specific host factors (xenognosins) in the plant pathogen Agrobacterium tumefaciens. Using whole cell assays, stable inhibitors inspired by the labile natural benzoxazinone inh... |
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Can phlorotannins purified extracts constitute a novel pharmacological alternative for microbial infections with associated inflammatory conditions?
PLoS ONE 7(2) , e31145, (2012) Bacterial and fungal infections and the emerging multidrug resistance are driving interest in fighting these microorganisms with natural products, which have generally been considered complementary to pharmacological therapies. Phlorotannins are polyphenols r... |
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Anti-proliferative activity and chemical characterization by comprehensive two-dimensional liquid chromatography coupled to mass spectrometry of phlorotannins from the brown macroalga Sargassum muticum collected on North-Atlantic coasts.
J. Chromatogr. A. 1428 , 115-25, (2016) In the present work, the phlorotannin composition of different Sargassum muticum samples collected at different locations along the North Atlantic coasts as well as the bioactivities related to these components were investigated. After pressurized liquid extr... |
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The ortho backbone amide linker (o-BAL) is an easily prepared and highly acid-labile handle for solid-phase synthesis.
J. Comb. Chem. 4(3) , 223-8, (2002) The tris(alkoxy)benzyl backbone amide linker (BAL) has found widespread application in solid-phase synthesis. The key intermediate for preparation of para BAL (p-BAL) is 2,6-dimethoxy-4-hydroxybenzaldehyde; several reports on its synthesis have appeared. Howe... |
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Enhancement of solubility by temporary dimethoxybenzyl-substitution of peptide bonds. Towards the synthesis of defined oligomers of alanine and of lysyl-glutamyl-glycine.
Int. J. Pept. Protein Res. 37(6) , 556-64, (1991) The synthesis of the model compound Aloc-Ala-Ala-Dma-Ala-Ala-OMe has been described as an illustration of the fact that a large group reversibly alkylating the amido group of an oligomer can disturb the regularity of a peptide backbone, oppose its aggregation... |