115983
Trimethyl 1,3,5-benzenetricarboxylate
98%
Synonym(s):
Trimesic acid trimethyl ester, Trimethyl trimesate
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About This Item
Linear Formula:
C6H3(CO2CH3)3
CAS Number:
Molecular Weight:
252.22
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
220-215-5
MDL number:
Product Name
Trimethyl 1,3,5-benzenetricarboxylate, 98%
InChI key
RGCHNYAILFZUPL-UHFFFAOYSA-N
InChI
1S/C12H12O6/c1-16-10(13)7-4-8(11(14)17-2)6-9(5-7)12(15)18-3/h4-6H,1-3H3
SMILES string
COC(=O)c1cc(cc(c1)C(=O)OC)C(=O)OC
assay
98%
form
solid
mp
145-147 °C (lit.)
functional group
ester
Quality Level
Related Categories
Application
Trimethyl 1,3,5-benzenetricarboxylate has been used to synthesize yttrium trimesates with open frameworks.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Bao-Xia Dong et al.
Dalton transactions (Cambridge, England : 2003), 39(24), 5683-5687 (2010-05-21)
Two novel yttrium trimesates with open frameworks have been synthesized by the self-assembly of trimethyl 1,3,5-benzenetricarboxylate and Y(3+) ion in mixed solvent of dimethylformamide (DMF)/water and diethylformamide (DEF)/water, where changes of solvents with different molecular sizes lead to the formation
Sheng-Mu You et al.
Nanomaterials (Basel, Switzerland), 10(9) (2020-09-02)
Photoelectrochemical (PEC) water splitting is a promising strategy to improve the efficiency of oxygen evolution reactions (OERs). However, the efficient adsorption of visible light as well as long-term stability of light-harvesting electrocatalysis is the crucial issue in PEC cells. Metal-organic
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