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115983

Sigma-Aldrich

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:
2672-58-4
Molecular Weight:
252.22
EC Number:
220-215-5
MDL number:
MFCD00008434
UNSPSC Code:
12352100
PubChem Substance ID:
24847255
NACRES:
NA.22

Quality Level

100

assay

98%

form

solid

mp

145-147 °C (lit.)

functional group

ester

SMILES string

COC(=O)c1cc(cc(c1)C(=O)OC)C(=O)OC

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

InChI key

RGCHNYAILFZUPL-UHFFFAOYSA-N

Related Categories

Application

Trimethyl 1,3,5-benzenetricarboxylate has been used to synthesize yttrium trimesates with open frameworks.

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)

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Certificates of Analysis (COA)

Lot/Batch Number
MKBV3428V
MKBQ4194V
MKBH6661V
MKBD6944
08202AJ

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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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