D132004
3,5-Dimethoxybenzoic acid
97%
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About This Item
Linear Formula:
(CH3O)2C6H3CO2H
CAS Number:
Molecular Weight:
182.17
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
214-473-8
Beilstein/REAXYS Number:
511834
MDL number:
Assay:
97%
Form:
powder
Quality Level
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
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
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Crystal structures, luminescence, and thermodynamic properties of lanthanide complexes with 3, 5-dimethoxybenzoic acid and 1, 10-phenanthroline.
Zheng JR, et al.
The Journal of Chemical Thermodynamics, 57(9), 169-177 (2013)
Protein sulfenation as a redox sensor: proteomics studies using a novel biotinylated dimedone analogue.
Charles RL, et al.
Molecular and Cellular Proteomics, 6(9), 1473-1484 (2007)
Rhodium-and iridium-catalyzed oxidative coupling of benzoic acids with alkynes via regioselective C- H bond cleavage.
Ueura K, et al.
The Journal of Organic Chemistry, 72(14), 5362-5367 (2007)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| D132004-25G | 04061831826432 |
| D132004-100G | 04061838353702 |