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Merck
CN

60730

Khellin

suitable for microscopy

Synonym(s):

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

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About This Item

Empirical Formula (Hill Notation):
C14H12O5
CAS Number:
Molecular Weight:
260.24
UNSPSC Code:
12171500
NACRES:
MA.02
PubChem Substance ID:
EC Number:
201-392-8
Beilstein/REAXYS Number:
263185
MDL number:
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assay

≥98.0% (HPLC)

Quality Level

form

powder

bp

180-200 °C/0.05 mmHg (lit.)

mp

150-154 °C (lit.)

suitability

suitable for microscopy

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

signalword

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

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

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges


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Fatma A Ragab et al.
European journal of medicinal chemistry, 42(8), 1117-1127 (2007-03-10)
The synthesis of 9- and 6-alkylaminomethyl furoflavones 5a, b, 9a-c, 13a, b, 15a-g and 18 from the naturally occurring chromones visnagin and khellin. Gastroprotective potency of these compounds in the ethanol damage model was determined. The results indicate that, through
Karin G Haug et al.
Planta medica, 78(17), 1831-1836 (2012-10-26)
The furanochromone visnagin is one of the main compounds of Ammi visnaga L. (syn. Khella) with potential effects on kidney stone prevention. After determination of the pharmacokinetic properties of visnagin after intravenous bolus administration in rats, the aim of the
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).
Nishit S Patel et al.
Dermatologic surgery : official publication for American Society for Dermatologic Surgery [et al.], 38(3), 381-391 (2012-02-01)
Vitiligo is an acquired multifocal and polygenic dyschromia that affects 1% to 3% of the world and presents as multiple depigmented macules and patches. Traditionally, the treatment of vitiligo has focused on pharmacologic interventions, but nearly half of all treated
Sally S El-Nakkady et al.
Acta poloniae pharmaceutica, 69(4), 645-655 (2012-08-11)
Bromination of visnaginone (1) yielded the dibromo derivative (2), which upon methylation with methyl iodide gave 1-(2,7-dibromo-4,6-dimethoxybenzofuran-5-yl) ethanone (3). Compound (3) reacted with dimethylformamide dimethylacetal to give (4). The reaction of (3) with aromatic aldehydes namely (vanillin, benzaldehyde and 3-anisaldehyde)

Global Trade Item Number

SKUGTIN
60730-10G04061832676609

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