230669
4-Phenoxyphenol
99%
Sinonimo/i:
Hydroquinone monophenyl ether
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About This Item
Formula condensata:
C6H5OC6H4OH
Numero CAS:
Peso molecolare:
186.21
Beilstein:
2047182
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
Livello qualitativo
Saggio
99%
Forma fisica
solid
Punto di fusione
80-84 °C (lit.)
Gruppo funzionale
phenoxy
Stringa SMILE
Oc1ccc(Oc2ccccc2)cc1
InChI
1S/C12H10O2/c13-10-6-8-12(9-7-10)14-11-4-2-1-3-5-11/h1-9,13H
ZSBDGXGICLIJGD-UHFFFAOYSA-N
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Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
338.0 °F - closed cup
Punto d’infiammabilità (°C)
170 °C - closed cup
Dispositivi di protezione individuale
dust mask type N95 (US), Eyeshields, Gloves
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In the biorefinery utilizing lignocellulosic biomasses, lignin decomposition to value-added phenolic derivatives is a key issue, and recently biocatalytic delignification is emerging owing to its superior selectivity, low energy consumption, and unparalleled sustainability. However, besides heme-containing peroxidases and laccases, information
Xiaolu Jiang et al.
Bioorganic & medicinal chemistry letters, 18(24), 6549-6552 (2008-10-28)
The synthesis and biological evaluation of a series of diphenyl ether derivatives were described. The compounds can either activate or inhibit the aminopeptidase activity of leukotriene A(4) hydrolase, while at the same time do not influence the hydrolase activity. Further
Cynthia D Selassie et al.
Journal of medicinal chemistry, 48(23), 7234-7242 (2005-11-11)
In this comprehensive study on the caspase-mediated apoptosis-inducing effect of 51 substituted phenols in a murine leukemia cell line (L1210), we determined the concentrations needed to induce caspase activity by 50% (I50) and utilized these data to develop the following
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