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文件

T68101

3′,4′,5′-三甲氧基苯乙酮

Name: 3′,4′,5′-三甲氧基苯乙酮
Brand: ALDRICH

98%

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线性分子式:

(CH₃O)₃C₆H₂COCH₃

CAS号:

1136-86-3

分子量:

210.23

Beilstein:

1463133

EC 号:

214-501-9

MDL编号:

MFCD00008738

PubChem化学物质编号:

24900407

NACRES:

NA.22

质量水平

100

检测方案

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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储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)

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Electrosprayed mesoporous particles for improved aqueous solubility of a poorly water soluble anticancer agent: in vitro and ex vivo evaluation.

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

Evidence for an alternative pathway for colchicine binding to tubulin, based on the binding kinetics of the constituent rings.

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)

Atropa belladonna hairy roots: orchestration of concurrent oxidation and reduction reactions for biotransformation of carbonyl compounds.

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

Selective valorization of lignin to phenol by direct transformation of Csp2-Csp3 and C-O bonds.

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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