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H23805

Sigma-Aldrich

4-Hydroxycoumarin

98%

Sinônimo(s):

4-Hydroxy-1-benzopyran-2-one

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About This Item

Fórmula empírica (Notação de Hill):
C9H6O3
Número CAS:
1076-38-6
Peso molecular:
162.14
Beilstein:
129768
Número CE:
214-060-2
Número MDL:
MFCD00006856
Código UNSPSC:
12352100
ID de substância PubChem:
24895160
NACRES:
NA.22

Ensaio

98%

pf

211-213 °C (lit.)

fluorescência

λem 373 nm in methanol

cadeia de caracteres SMILES

OC1=CC(=O)Oc2ccccc12

InChI

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

chave InChI

VXIXUWQIVKSKSA-UHFFFAOYSA-N

Informações sobre genes

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

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Categorias relacionadas

Pictogramas

Exclamation mark
GHS07

Palavra indicadora

Warning

Frases de perigo

H302

Declarações de precaução

P264 - P270 - P301 + P312 - P501

Classificações de perigo

Acute Tox. 4 Oral

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves

Certificados de análise (COA)

Busque Certificados de análise (COA) digitando o Número do Lote do produto. Os números de lote e remessa podem ser encontrados no rótulo de um produto após a palavra “Lot” ou “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

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
Ian A Nicholls et al.
Journal of molecular recognition : JMR, 23(6), 604-608 (2010-10-30)
The complex nature of the structure of the anticoagulant warfarin is reflected in the diversity of binding modes observed in warfarin-protein recognition systems. A series of theoretical, (1)H-NMR and steady state and time resolved fluorescence spectroscopic studies, have been used
Yan Sun et al.
Molecular diversity, 16(1), 163-171 (2011-12-01)
An efficient synthetic method for the densely substituted 3-arylaminoacrylates was successfully developed via the one-pot reaction of arylamines, methyl propiolate, aromatic aldehydes, and active methylene compounds such as pivaloylacetonitrile, 1,3-cyclopentanedione, and 4-hydroxycoumarin. The key step of the reaction was believed
Davorka Završnik et al.
Molecules (Basel, Switzerland), 16(7), 6023-6040 (2011-07-21)
We report on the synthesis of 4-hydroxycoumarin dimers 1-15 bearing an aryl substituent on the central linker and fused benzopyranocoumarin derivatives 16-20 and on their in vitro broad anti-DNA and RNA virus activity evaluations. The chemical identities and structure of
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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