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630586

2′-Hydroxy-4′,6′-dimethoxyacetophenone

Name: 2′-Hydroxy-4′,6′-dimethoxyacetophenone
Brand: ALDRICH

97%

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About This Item

Empirical Formula (Hill Notation):

C₁₀H₁₂O₄

CAS Number:

90-24-4

Molecular Weight:

196.20

NACRES:

NA.22

PubChem Substance ID:

24882306

UNSPSC Code:

12352100

EC Number:

201-978-3

MDL number:

MFCD00017243

Assay:

97%

Form:

solid

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Properties

Quality Level

100

assay

97%

form

solid

mp

80-84 °C (lit.)

functional group

ketone

SMILES string

COc1cc(O)c(C(C)=O)c(OC)c1

InChI

1S/C10H12O4/c1-6(11)10-8(12)4-7(13-2)5-9(10)14-3/h4-5,12H,1-3H3

InChI key

FBUBVLUPUDBFME-UHFFFAOYSA-N

Description

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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Molecular structure and QSAR study on antispasmodic activity of some xanthoxyline derivatives.

Rodrigo dos Santos et al.

Archiv der Pharmazie, 339(5), 227-237 (2006-03-31)

Semi-empirical molecular orbital calculations at AM1 level were done with the aim to investigate the structure-activity relationships of antispasmodic activities of ten 2-(X-benzyloxy)-4,6-dimethoxyacetophenones with X = H, 4'-F, 4'-NO2, 4'-CH3, 4'-Cl, 3',4'-(CH3)2, 4'-OCH3, 4'-Br, 4'-OCH2C6H5, and 4'-C(CH3)3, against acetylcholine-induced contraction

Fungicide and fungiostatic effects of xanthoxyline.

V Cechinel Filho et al.

Journal of ethnopharmacology, 53(3), 171-173 (1996-09-01)

Antifungal activity and studies on mode of action of novel xanthoxyline-derived chalcones.

Paula Boeck et al.

Archiv der Pharmazie, 338(2-3), 87-95 (2005-03-31)

Chalcones and chalcone-like compounds, most of them new ones, prepared by base-catalyzed condensation of appropriate aldehydes and xanthoxyline, were tested for antifungal properties against a panel of yeasts, hialohyphomycetes as well as dermatophytes with the agar dilution assay. Results indicate

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Global Trade Item Number

SKU	GTIN
630586-5G	04061832713984