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Merck
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Key Documents

Altri documenti

H23805

Sigma-Aldrich

4-Hydroxycoumarin

98%

Sinonimo/i:

4-Hydroxy-1-benzopyran-2-one

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About This Item

Formula empirica (notazione di Hill):
C9H6O3
Numero CAS:
1076-38-6
Peso molecolare:
162.14
Beilstein:
129768
Numero CE:
214-060-2
Numero MDL:
MFCD00006856
Codice UNSPSC:
12352100
ID PubChem:
24895160
NACRES:
NA.22

Saggio

98%

Punto di fusione

211-213 °C (lit.)

Fluorescenza

λem 373 nm in methanol

Stringa SMILE

OC1=CC(=O)Oc2ccccc12

InChI

1S/C9H6O3/c10-7-5-9(11)12-8-4-2-1-3-6(7)8/h1-5,10H
VXIXUWQIVKSKSA-UHFFFAOYSA-N

Informazioni sul gene

mouse ... Maoa(17161)
rat ... Aldh1a2(116676)

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Categorie correlate

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H302

Classi di pericolo

Acute Tox. 4 Oral

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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4-Hydroxy-7-methylcoumarin AldrichCPR

Sigma-Aldrich

IDF00004

4-Hydroxy-7-methylcoumarin

3-(α-Acetonylbenzyl)-4-hydroxycoumarin sodium salt ≥98%

Sigma-Aldrich

A4571

3-(α-Acetonylbenzyl)-4-hydroxycoumarin sodium salt

Karen A Nolan et al.
Journal of medicinal chemistry, 52(22), 7142-7156 (2009-11-03)
The synthesis is reported here of two novel series of inhibitors of human NAD(P)H quinone oxidoreductase-1 (NQO1), an enzyme overexpressed in several types of tumor cell. The first series comprises substituted symmetric dicoumarol analogues; the second series contains hybrid compounds
Ayoob Bazgir et al.
Ultrasonics sonochemistry, 17(2), 447-452 (2009-10-20)
A simple, facile, efficient and three-component procedure for the synthesis of spiro[indoline-3,4'-pyrazolo[3,4-b]pyridine]-2,6'(1'H)-diones by the reaction of 4-hydroxycumarin, isatins and 1H-pyrazol-5-amines in water under ultrasonic irradiation is reported. The advantages of this method are the use of an inexpensive and readily
Mikael I Naumov et al.
The Journal of organic chemistry, 72(9), 3293-3301 (2007-03-29)
2-(methoxymethoxymethyl)aryllead triacetates, obtained in situ from the corresponding arylboronic acids, reacted with 4-hydroxycoumarins, leading to 3-(2-methoxymethoxymethyl)aryl-4-hydroxycoumarin derivatives in good to high yields. These compounds underwent a cascade sequence of reactions, deprotection-halogenation-annulation, to afford polyoxygenated tetracyclic 6H,11H-[2]benzopyrano-[4,3-c] [1]benzopyran-11-ones in good yields.
Katrin J Czogalla et al.
Blood, 122(15), 2743-2750 (2013-08-29)
Since the discovery of warfarin-sensitive vitamin K 2,3-epoxide reductase complex subunit 1 (VKORC1), 26 human VKORC1 (hVKORC1) missense mutations have been associated with oral anticoagulant resistance (OACR). Assessment of warfarin resistance using the "classical" dithiothreitol-driven vitamin K 2,3-epoxide reductase (VKOR)
Benye Liu et al.
Plant molecular biology, 72(1-2), 17-25 (2009-09-17)
Coumarin forms in melilotoside (trans-ortho-coumaric acid glucoside)-containing plant species upon cell damage. In moldy melilotoside-containing plant material, trans-ortho-coumaric acid is converted by fungi to 4-hydroxycoumarin, two molecules of which spontaneously combine with formaldehyde to give dicoumarol. Dicoumarol causes internal bleeding
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