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T70602

Sigma-Aldrich

3,4,5-Trimethoxyphenylacetic acid

97%

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About This Item

Linear Formula:
(CH3O)3C6H2CH2CO2H
CAS Number:
951-82-6
Molecular Weight:
226.23
Beilstein/REAXYS Number:
2697844
EC Number:
213-456-2
MDL number:
MFCD00004336
UNSPSC Code:
12352100
PubChem Substance ID:
24900247
NACRES:
NA.22

assay

97%

mp

117-120 °C (lit.)

SMILES string

COc1cc(CC(O)=O)cc(OC)c1OC

InChI

1S/C11H14O5/c1-14-8-4-7(6-10(12)13)5-9(15-2)11(8)16-3/h4-5H,6H2,1-3H3,(H,12,13)

InChI key

DDSJXCGGOXKGSJ-UHFFFAOYSA-N

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Related Categories

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Ahmet Şenocak et al.
Dalton transactions (Cambridge, England : 2003), 47(29), 9617-9626 (2018-07-04)
The synthesis and characterization of new hybrid materials based on reduced graphene oxide (rGO) or single walled carbon nanotubes (SWCNTs) covalently functionalized by 4,4'-difluoro-8-(4-propynyloxy)-phenyl-1,3,5,7-tetramethyl-4-bora-3a,4a-diaza-s-indacene (BODIPY) (2) or 7-(prop-2-yn-1-yloxy)-3-(3',4',5'-trimethoxyphenyl)-coumarin (4) as light harvesting groups have been described. The organic solar cell
M I Donnelly et al.
Journal of bacteriology, 147(2), 477-481 (1981-08-01)
When grown at the expense of 3,4,5-trimethoxyphenylacetic acid, a species of Arthrobacter readily oxidized 3,4-dihydroxy-5-methoxyphenylacetic acid, but other structurally related aromatic acids were oxidized only slowly. Cell extracts contained a dioxygenase for 3,4-dihydroxy-5-methoxyphenylacetate, and the corresponding trihydroxy acid, which was

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