D132004
3,5-Dimethoxybenzoic acid
97%
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About This Item
Productos recomendados
assay
97%
form
powder
mp
178-180 °C (lit.)
SMILES string
COc1cc(OC)cc(c1)C(O)=O
InChI
1S/C9H10O4/c1-12-7-3-6(9(10)11)4-8(5-7)13-2/h3-5H,1-2H3,(H,10,11)
InChI key
IWPZKOJSYQZABD-UHFFFAOYSA-N
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Application
3,5-Dimethoxybenzoic acid (3,5-DmeoxBA) can be used as a reactant for the synthesis of:
It can also be used as a ligand to synthesize lanthanide complexes [Ln(3,5-DmeoxBA)3(phen)]2; where phen is 1,10-phenanthroline.
- 5,7-Dimethoxy-3,4-diphenylisocoumarin by coupling with diphenylacetylene.
- Biotin dimedone, a reagent used in the study of protein sulfenation.
It can also be used as a ligand to synthesize lanthanide complexes [Ln(3,5-DmeoxBA)3(phen)]2; where phen is 1,10-phenanthroline.
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Protein sulfenation as a redox sensor: proteomics studies using a novel biotinylated dimedone analogue.
Molecular and Cellular Proteomics, 6(9), 1473-1484 (2007)
Crystal structures, luminescence, and thermodynamic properties of lanthanide complexes with 3, 5-dimethoxybenzoic acid and 1, 10-phenanthroline.
The Journal of Chemical Thermodynamics, 57(9), 169-177 (2013)
European journal of medicinal chemistry, 100, 119-128 (2015-06-17)
A series of 2-(4-R-triazolyl)substituted 3-oxo-2,3-dihydrofurocoumarins have been synthesized by a regioselective cycloaddition of 2-azidooreoselone 1 or 2-azido-9-[(4-methylpiperazin-1-yl)methyl]oreoselone 2 with various alkynes in the presence of Cu(II)/ascorbate in water/methylene chloride reaction medium. The structure of 2-azidooreoselone was established by X-ray structure
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