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Key Documents

60730

Sigma-Aldrich

Khellin

for microscopy

Synonym(s):

4,9-Dimethoxy-7-methyl-5H-furo[3,2-g][1]benzopyran-5-one

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10 G
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10 G
€215.00

About This Item

Empirical Formula (Hill Notation):
C14H12O5
CAS Number:
Molecular Weight:
260.24
Beilstein:
263185
EC Number:
MDL number:
UNSPSC Code:
12171500
PubChem Substance ID:
NACRES:
MA.02

€215.00


Estimated to ship on13 May 2025


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grade

for microscopy

Quality Level

Assay

≥98.0% (HPLC)

form

powder

bp

180-200 °C/0.05 mmHg (lit.)

mp

150-154 °C (lit.)

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

room temp

SMILES string

COc1c2OC(C)=CC(=O)c2c(OC)c3ccoc13

InChI

1S/C14H12O5/c1-7-6-9(15)10-11(16-2)8-4-5-18-12(8)14(17-3)13(10)19-7/h4-6H,1-3H3

InChI key

HSMPDPBYAYSOBC-UHFFFAOYSA-N

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Pictograms

Skull and crossbones

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

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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Jin-Koo Lee et al.
Archives of pharmacal research, 33(11), 1843-1850 (2010-12-01)
Visnagin, which is found in Ammi visnaga, has biological activity as a vasodilator and reduces blood pressure by inhibiting calcium influx into the cell. The present study demonstrates the anti-inflammatory effect of visnagin on lipopolysaccharide (LPS)-stimulated BV-2 microglial cells. When
Jaap de Leeuw et al.
European journal of dermatology : EJD, 13(5), 474-477 (2003-12-25)
Vitiligo destroys the melanocytes in the epidermis; the inactive melanocytes in the outer root sheaths are not affected. Phosphatidylcholine liposomes are able to target molecules contained in them into the hair follicles. Khellin is activated by UVA and previous studies
Salama Omar et al.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 8(8), 1179-1186 (2009-07-30)
A theoretical investigation of the formation and spectroscopic properties of the furan and pyrone monoadducts between the photosensitizer khellin and DNA base thymine is reported. The thermal reaction pathways involve very high barriers, whereas the excited state surfaces display low
Ameen Ali Abu-Hashem et al.
Molecules (Basel, Switzerland), 16(3), 1956-1972 (2011-03-02)
6-[(4-Methoxy/4,9-dimethoxy)-7-methylfurochromen-5-ylideneamino]-2-thioxo-2,3-dihydropyrimidin-4-ones 1a,b were prepared by reaction of 6-amino-2-thiouracil with visnagen or khellin, respectively. Reaction of 1a,b with methyl iodide afforded furochromenylideneaminomethylsulfanylpyrimidin-4-ones 2a,b. Compounds 2a,b were reacted with secondary aliphatic amines to give the corresponding furochromen-ylideneamino-2-substituted pyrimidin-4-ones 3a-d. Reaction of 3a-d
Omaima Mohamed Abdelhafez et al.
Archives of pharmacal research, 34(10), 1623-1632 (2011-11-15)
Bromination of visnagin (1) afforded 9-bromovisnagin (2) which on its alkaline hydrolysis afforded the 3-acetyl benzofuran derivative (3). The condensation of (3) with hydrazine hydrate, phenylhydrazine and/or hydroxylamine hydrochloride afforded the corresponding pyrazole derivatives (4a, b) and isoxazole derivative (4c).

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