183725
4-(Imidazol-1-yl)phenol
97%
Sinônimo(s):
1-(4-Hydroxyphenyl)imidazole
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About This Item
Fórmula empírica (Notação de Hill):
C9H8N2O
Número CAS:
Peso molecular:
160.17
Número CE:
Número MDL:
Código UNSPSC:
12352005
ID de substância PubChem:
NACRES:
NA.22
Produtos recomendados
Nível de qualidade
Ensaio
97%
Formulário
powder
pf
204-206 °C (lit.)
cadeia de caracteres SMILES
Oc1ccc(cc1)-n2ccnc2
InChI
1S/C9H8N2O/c12-9-3-1-8(2-4-9)11-6-5-10-7-11/h1-7,12H
chave InChI
CYKCUAPYWQDIKR-UHFFFAOYSA-N
Aplicação
4-(Imidazol-1-yl)phenol was used in evaluation of estrogenicity of phenolic xenoestrogens by Saccharomyces cerevisiae-based Lac-Z reporter assay.
Palavra indicadora
Warning
Frases de perigo
Declarações de precaução
Classificações de perigo
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Órgãos-alvo
Respiratory system
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
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Journal of fluorescence, 27(6), 2159-2168 (2017-09-10)
The interaction of n-(4-hydroxyphenyl)-imidazole with p-sulfonatocalix[4]arene is studied using fluorescence technique. The quenching of fluorescence intensity explains the efficiency of binding via binding constant and quenching constant. The excited state lifetime of n-(4-hydroxyphenyl)-imidazole is decreased upon interaction with p-sulfonatocalix[4]arene. The
Effect of substituent size and dimensionality on potency of phenolic xenoestrogens evaluated with a recombinant yeast assay.
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In this study, a molecularly imprinted polymer capable of recognizing 8 benzimidazoles was first synthesized. The computation simulation showed that the shape and size of used template were the main factors influencing its recognition ability. Then the polymer was used
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 183725-5G | |
| 183725-1G | 4061826652428 |
| 183725-25G |
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