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Merck
Tutte le immagini(1)

Documenti fondamentali

60730

Sigma-Aldrich

Khellin

for microscopy

Sinonimo/i:

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

Autenticatiper visualizzare i prezzi riservati alla tua organizzazione & contrattuali


About This Item

Formula empirica (notazione di Hill):
C14H12O5
Numero CAS:
Peso molecolare:
260.24
Beilstein:
263185
Numero CE:
Numero MDL:
Codice UNSPSC:
12171500
ID PubChem:
NACRES:
MA.02

Grado

for microscopy

Livello qualitativo

Saggio

≥98.0% (HPLC)

Stato

powder

P. ebollizione

180-200 °C/0.05 mmHg (lit.)

Punto di fusione

150-154 °C (lit.)

Compatibilità

suitable for microscopy

applicazioni

diagnostic assay manufacturing
hematology
histology

Temperatura di conservazione

room temp

Stringa SMILE

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
HSMPDPBYAYSOBC-UHFFFAOYSA-N

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Pittogrammi

Skull and crossbones

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

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

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

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

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

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


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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)
Rosita Saraceno et al.
Dermatologic therapy, 22(4), 391-394 (2009-07-08)
Vitiligo is an acquired depigmentation disorder affecting 1-4% of the world's population. Conventional therapies include steroids, photosensitive topical agents, surgical treatments, and phototherapy. The aim of the study was to evaluate the efficacy of monochromatic excimer light 308 nm (MEL)
P Vanachayangkul et al.
Urological research, 39(3), 189-195 (2010-11-12)
In Egypt, teas prepared from the fruits of Ammi visnaga L. (syn. "Khella") are traditionally used by patients with urolithiasis. The aim of this study was to evaluate whether oral administration of an aqueous extract prepared from the fruits of
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

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