![]() 3,5-Dimethoxybenzaldehyde structure
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Common Name | 3,5-Dimethoxybenzaldehyde | ||
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CAS Number | 7311-34-4 | Molecular Weight | 166.17 | |
Density | 1.1±0.1 g/cm3 | Boiling Point | 276.5±0.0 °C at 760 mmHg | |
Molecular Formula | C9H10O3 | Melting Point | 45-48 °C(lit.) | |
MSDS | Chinese USA | Flash Point | 119.0±8.2 °C | |
Symbol |
![]() GHS07 |
Signal Word | Warning |
Recoverable PEG-supported copper catalyst for highly stereocontrolled nitroaldol condensation.
Org. Lett. 9 , 2151, (2007) A new poly(ethylene glycol)-modified DAT2-Cu(OAc)2 complex smoothly catalyzes a base-free nitroaldol condensation in a highly enantioselective manner (ee up to 93%) also in reagent-grade solvent and in the presence of air. Effective recovery and recycling (up... |
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A cyclopropanol-based strategy for subunit coupling: total synthesis of (+)-spirolaxine methyl ether.
Org. Lett. 9 , 2717, (2007) A strategy for ketone synthesis with cyclopropanols as intermediates and its application to (+)-spirolaxine methyl ether is described. The synthesis also features an application of Fu's alkyl-alkyl Suzuki coupling. |
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An expedient synthesis of 5-n-alkylresorcinols and novel 5-n-alkylresorcinol haptens.
Beilstein J. Org. Chem. 5 , 22, (2009) The first synthesis of bioactive long alkyl chain 5-n-alkylresorcinols, present in whole grain products, by a novel modification of the Wittig reaction is described. All the main long chain 5-n-alkylresorcinols present in rye and wheat, including C(23) and C(... |
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Synthesis, structure and theoretical investigation into a homoleptic tris(dithiolene) tungsten.
Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 120C , 208-215, (2013) A new homoleptic dithiolene tungsten complex, tris-{1,2-bis(3,5-dimethoxyphenyl)-1,2-ethylenodithiolene-S,S'}tungsten, was successfully synthesized via a reaction of the thiophosphate ester and sodium tungstate. The thiophosphate ester was prepared from 3,5-d... |
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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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