4-Phenoxyphenol structure
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Common Name | 4-Phenoxyphenol | ||
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CAS Number | 831-82-3 | Molecular Weight | 186.207 | |
Density | 1.2±0.1 g/cm3 | Boiling Point | 313.8±25.0 °C at 760 mmHg | |
Molecular Formula | C12H10O2 | Melting Point | 80-84 °C(lit.) | |
MSDS | Chinese USA | Flash Point | 141.4±17.4 °C |
Use of 4-PhenoxyphenolBIF-44, also known as 4-Phenoxyphenol and Hydroquinone monophenyl ether, is a sensitizer of BCL-2-associated X protein (BAX) activation by binding to a pocket formed by the junction of the α3-α4 and α5-α6 hairpins. BIF-44 enhances BAX activity. |
Name | 4-phenoxyphenol |
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Synonym | More Synonyms |
Density | 1.2±0.1 g/cm3 |
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Boiling Point | 313.8±25.0 °C at 760 mmHg |
Melting Point | 80-84 °C(lit.) |
Molecular Formula | C12H10O2 |
Molecular Weight | 186.207 |
Flash Point | 141.4±17.4 °C |
Exact Mass | 186.068085 |
PSA | 29.46000 |
LogP | 3.35 |
Vapour Pressure | 0.0±0.7 mmHg at 25°C |
Index of Refraction | 1.605 |
Stability | Stable. Combustible. Incompatible with strong oxidizing agents. |
Water Solubility | insoluble |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
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Hazard Codes | Xi:Irritant |
Risk Phrases | R36/37/38 |
Safety Phrases | S26-S36-S37/39 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
Packaging Group | I; II; III |
HS Code | 29095090 |
Precursor 10 | |
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DownStream 10 | |
HS Code | 2909500000 |
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Summary | 2909500000 ether-phenols, ether-alcohol-phenols and their halogenated, sulphonated, nitrated or nitrosated derivatives VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0% |
Cellular apoptosis and cytotoxicity of phenolic compounds: a quantitative structure-activity relationship study.
J. Med. Chem. 48 , 7234-42, (2005) 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 caspas... |
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Activation and inhibition of leukotriene A4 hydrolase aminopeptidase activity by diphenyl ether and derivatives.
Bioorg. Med. Chem. Lett. 18 , 6549-52, (2008) 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... |
4-Phenoxyphenol |
o-Phenylhydroquinone |
EINECS 212-611-1 |
MFCD00002331 |
Phenol, 4-phenoxy- |