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64951

7-Methoxycoumarin

Name: 7-Methoxycoumarin
Brand: SIGMA

suitable for fluorescence, ≥98.0% (TLC)

Synonym(s):

Herniarin, Methyl umbelliferyl ether

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About This Item

Empirical Formula (Hill Notation):

C₁₀H₈O₃

CAS Number:

531-59-9

Molecular Weight:

176.17

UNSPSC Code:

85151701

NACRES:

NA.32

PubChem Substance ID:

57651999

EC Number:

208-513-3

Beilstein/REAXYS Number:

141728

MDL number:

MFCD00006876

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Properties

Quality Level

100

assay

≥98.0% (TLC)

form

solid

mp

117-121 °C (lit.)

solubility

DMF: soluble, acetonitrile: soluble, alcohols: soluble, chloroform: soluble

fluorescence

λ_ex 350 nm; λ_em 385 nm (Reaction product), λ_ex 350 nm; λ_em 385 nm in chloroform

suitability

suitable for fluorescence

SMILES string

COc1ccc2C=CC(=O)Oc2c1

InChI

1S/C10H8O3/c1-12-8-4-2-7-3-5-10(11)13-9(7)6-8/h2-6H,1H3

InChI key

LIIALPBMIOVAHH-UHFFFAOYSA-N

Description

Application

7-Methoxycoumarin (Herniarin) is used to study antioxidant and hepatoprotective properties and its activity as an allergen. 7-Methoxycoumarin may be used as a reference material in the purification, separation and analysis of coumarin compounds.

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Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Ameliorative effects of 7-methylcoumarin and 7-methoxycoumarin against CCl4-induced hepatotoxicity in rats.

Sandesh Sancheti et al.

Drug and chemical toxicology, 36(1), 42-47 (2012-11-07)

The available conventional remedies for the treatment of drug-induced liver diseases are highly inadequate and possess serious adverse effects; therefore, the development of new, effective drugs is considered necessary. This article explores the hepatoprotective and antioxidant potential of 7-methylcoumarin (MC)

Acceleration of 7-[methoxy-14C]coumarin-derived carbon dioxide exhalation by cobalt pretreatment in mice.

W Legrum et al.

The Journal of pharmacology and experimental therapeutics, 221(3), 790-794 (1982-06-01)

Pretreatment of rats with cobaltous chloride has been shown previously to reduce the content of cytochrome P-450 in the hepatic microsomal protein. This is accompanied by a corresponding decrease in substrate oxidation, e.g. ethyl morphine demethylation, in vitro. The present

[Studies on chemical constituents in herb from Artemisia rupestris].

Wei-Xia Song et al.

Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica, 31(21), 1790-1792 (2007-01-31)

To study the chemical constituents of Artemisia rupestris. The chemical constituents were isolated by column chromatography on silical gel and sephadex LH - 20. Their structures were elucidated on the basis of spectral analysis. 8 compounds have isolated from this

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Global Trade Item Number

SKU	GTIN
64951-100MG	04061832532806
64951-500MG	04061832532813