230669
4-Phenoxyphenol
99%
Sinónimos:
Hydroquinone monophenyl ether
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About This Item
Productos recomendados
Quality Level
assay
99%
form
solid
mp
80-84 °C (lit.)
functional group
phenoxy
SMILES string
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
InChI key
ZSBDGXGICLIJGD-UHFFFAOYSA-N
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Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
338.0 °F - closed cup
flash_point_c
170 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
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One of the key challenges in renewable chemical production is the conversion of lignin, especially by fast pyrolysis. The complexity of the lignin pyrolysis process has hindered the elucidation of the mechanism, inhibiting further industrial implementation. By combining pyrolysis of
Biotechnology for biofuels, 10, 212-212 (2017-09-16)
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
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
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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