189790
2,3,4-Trimethoxybenzoic acid
≥98%
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About This Item
Formula condensata:
(CH3O)3C6H2CO2H
Numero CAS:
Peso molecolare:
212.20
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
![1,8-diazabiciclo[5.4.0]undec-7-ene 98%](/deepweb/assets/sigmaaldrich/product/structures/120/564/5b373e23-1624-489c-8efb-692de0f96ffb/640/5b373e23-1624-489c-8efb-692de0f96ffb.png)
Saggio
≥98%
Stato
solid
Punto di fusione
99-102 °C (lit.)
Gruppo funzionale
carboxylic acid
Stringa SMILE
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)
HZNQSWJZTWOTKM-UHFFFAOYSA-N
Applicazioni
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.
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Dispositivi di protezione individuale
Eyeshields, Gloves, type N95 (US)
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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
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
An oxazoline based approach to (S)-Gossypol.
Meyers AI and Willemsen JJ.
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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)
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