189790
2,3,4-Trimethoxybenzoic acid
≥98%
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About This Item
Linear Formula:
(CH3O)3C6H2CO2H
CAS Number:
Molecular Weight:
212.20
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
209-350-0
MDL number:
Assay:
≥98%
Form:
solid
Quality Level
assay
≥98%
form
solid
mp
99-102 °C (lit.)
functional group
carboxylic acid
SMILES string
COc1ccc(C(O)=O)c(OC)c1OC
InChI
1S/C10H12O5/c1-13-7-5-4-6(10(11)12)8(14-2)9(7)15-3/h4-5H,1-3H3,(H,11,12)
InChI key
HZNQSWJZTWOTKM-UHFFFAOYSA-N
Application
2,3,4-Trimethoxybenzoic acid was used in the synthesis of tropoloisoquinoline alkaloid pareitropone. It was also used in the synthesis of isomeric tris(pyrogallol) derivatives and naphthoic acid.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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Synthesis and characterization of a series of vanadium-tunichrome B 1 analogs. Crystal structure of a tris (catecholamide) complex of vanadium.
Bulls AR, et al.
Journal of the American Chemical Society, 112(7), 2627-2632 (1990)
Hung-Sheng Soung et al.
Neurotoxicity research, 34(3), 375-387 (2018-04-10)
Reserpine (RES)-induced orofacial dyskinesia (OD) has been used as an animal model for human tardive dyskinesia (TD) for decades, due to its strong pathophysiological association with striatal oxidative stress and neural cytoarchitecture alteration. L-Theanine (LT), one of the major amino
Ken S Feldman et al.
Journal of the American Chemical Society, 124(39), 11600-11601 (2002-09-26)
The synthesis of the tropoloisoquinoline alkaloid pareitropone has been accomplished in 14 steps from 2,3,4-trimethoxybenzoic acid. The key transformations include the generation of an alkylidenecarbene intermediate through intramolecular addition of a tosylamide anion to an alkynyliodonium salt, and the cycloaddition
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 189790-25G | 04061838759351 |