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T68101

Sigma-Aldrich

3′,4′,5′-Trimethoxyacetophenone

98%

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Linear Formula:
(CH3O)3C6H2COCH3
CAS Number:
1136-86-3
Molecular Weight:
210.23
Beilstein:
1463133
EC Number:
214-501-9
MDL number:
MFCD00008738
PubChem Substance ID:
24900407
NACRES:
NA.22

Quality Level

100

Assay

98%

bp

173-174 °C/10 mmHg (lit.)

mp

78-80 °C (lit.)

SMILES string

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

InChI

1S/C11H14O4/c1-7(12)8-5-9(13-2)11(15-4)10(6-8)14-3/h5-6H,1-4H3

InChI key

VUGQIIQFXCXZJU-UHFFFAOYSA-N

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Related Categories

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Y Engelborghs et al.
The Journal of biological chemistry, 268(1), 107-112 (1993-01-05)
The kinetics of tropolone methyl ether binding to tubulin were measured by following the loss of colchicine binding capacity upon preincubation of tubulin with tropolone methyl ether. At 25 degrees C a bimolecular association rate constant of 2.7 (+/- 0.2)
Elshaimaa Sayed et al.
Journal of controlled release : official journal of the Controlled Release Society, 278, 142-155 (2018-04-02)
Encapsulation of poorly water-soluble drugs into mesoporous materials (e.g. silica) has evolved as a favorable strategy to improve drug solubility and bioavailability. Several techniques (e.g. spray drying, solvent evaporation, microwave irradiation) have been utilized for the encapsulation of active pharmaceutical
Vikas Srivastava et al.
Applied biochemistry and biotechnology, 166(6), 1401-1408 (2012-01-17)
The biotransformation potential of a selected Atropa belladonna hairy root clone (AB-09) had been evaluated with regard to three different aromatic carbonyl compounds, i.e., 3,4,5-trimethoxybenzaldehyde (1), 3,4,5-trimethoxyacetophenone (2), and 3,4,5-trimethoxy benzoic acid (3). The results demonstrated for the first time
Jiang Yan et al.
Science advances, 6(45) (2020-11-08)
Phenol is an important commodity chemical in the industry, which is currently produced using fossil feedstocks. Here, we report a strategy to produce phenol from lignin by directly deconstructing Csp2-Csp3 and C-O bonds under mild conditions. It was found that

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