T68101
3′,4′,5′-Trimethoxyacetophenone
98%
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About This Item
Linear Formula:
(CH3O)3C6H2COCH3
CAS Number:
Molecular Weight:
210.23
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
214-501-9
Beilstein/REAXYS Number:
1463133
MDL number:
Product Name
3′,4′,5′-Trimethoxyacetophenone, 98%
InChI key
VUGQIIQFXCXZJU-UHFFFAOYSA-N
InChI
1S/C11H14O4/c1-7(12)8-5-9(13-2)11(15-4)10(6-8)14-3/h5-6H,1-4H3
SMILES string
COc1cc(cc(OC)c1OC)C(C)=O
assay
98%
bp
173-174 °C/10 mmHg (lit.)
mp
78-80 °C (lit.)
Quality Level
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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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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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