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assay
≥98%
form
solid
mp
99-102 °C (lit.)
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_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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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
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
Synthesis and characterization of a series of vanadium-tunichrome B 1 analogs. Crystal structure of a tris (catecholamide) complex of vanadium.
Journal of the American Chemical Society, 112(7), 2627-2632 (1990)
An oxazoline based approach to (S)-Gossypol.
Tetrahedron, 54(35), 10493-10511 (1998)
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