m-Methoxyphenol
m-Methoxyphenol structure
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Common Name | m-Methoxyphenol | ||
|---|---|---|---|---|
| CAS Number | 150-19-6 | Molecular Weight | 124.137 | |
| Density | 1.1±0.1 g/cm3 | Boiling Point | 244.3±0.0 °C at 760 mmHg | |
| Molecular Formula | C7H8O2 | Melting Point | -17 °C | |
| MSDS | USA | Flash Point | 119.1±4.8 °C | |
| Symbol |
GHS05, GHS06 |
Signal Word | Danger | |
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Convenient QSAR model for predicting the complexation of structurally diverse compounds with β-cyclodextrins
Bioorg. Med. Chem. 17 , 896-904, (2009) This paper reports a QSAR study for predicting the complexation of a large and heterogeneous variety of substances (233 organic compounds) with beta-cyclodextrins (beta-CDs). Several different theoretical molecular descriptors, calculated solely from the mole... |
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Calculating virtual log P in the alkane/water system (log P(N)(alk)) and its derived parameters deltalog P(N)(oct-alk) and log D(pH)(alk).
J. Med. Chem. 48 , 3269-79, (2005) Growing interest in the use of both the logarithm of the partition coefficient of the neutral species in the alkane/water system (log P(N)(alk)) and the difference between log P(N)(oct) (the logarithm of the partition coefficient of the neutral species in the... |
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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 caspase activity by 50% (I50) and utilized these data to develop ... |
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Action mechanism of tyrosinase on meta- and para-hydroxylated monophenols.
Biol. Chem. 381(4) , 313-20, (2000) The relationship between the structure and activity of meta- and para-hydroxylated monophenols was studied during their tyrosinase-catalysed hydroxylation and the rate-limiting steps of the reaction mechanism were identified. The para-hydroxylated substrates ... |
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Isolation and characterization of a veratrol:corrinoid protein methyl transferase from Acetobacterium dehalogenans.
Arch. Microbiol. 175(5) , 376-83, (2001) From 3-methoxyphenol-grown cells of Acetobacterium dehalogenans, an inducible enzyme was purified that mediated the transfer of the methyl groups of veratrol (1,2-dimethoxybenzene) to a corrinoid protein enriched from the same cells. In this reaction, veratro... |
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Combined injection of three different lineages of early-differentiating human amniotic fluid-derived cells restores urethral sphincter function in urinary incontinence.
BJU Int. 114(5) , 770-83, (2014) To investigate whether a triple combination of early-differentiated cells derived from human amniotic fluid stem cells (hAFSCs) would show synergistic effects in urethral sphincter regeneration.We early-differentiated hAFSCs into muscle, neuron and endothelia... |
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Oxidative and non-oxidative metabolism of 4-iodoanisole by rat liver microsomes.
Xenobiotica 25(2) , 143-50, (1995) 1. The oxidative metabolism of 4-iodoanisole (1) by liver microsomes from beta-naphthoflavone-treated rats yields 4-iodophenol (2) 2-iodo-5-methoxyphenol (3), 2-methoxy-5-iodophenol (4), 4-methoxyphenol (5), and 3-methoxyphenol (6) in relative yields of 5:2:4... |
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Facile lewis acid catalyzed synthesis of C(4) symmetric resorcinarenes
Org. Lett. 2(24) , 3869-71, (2000) The Lewis acid catalyzed condensation of 3-methoxyphenol with octanal produced the C(4) symmetric calix[4]resorcinarene 2, in high yield. Of the numerous stereo- and regioisomers possible, the rccc isomer with C(4) symmetry was the only product isolated (as a... |
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Metabolic activation of 3-hydroxyanisole by isolated rat hepatocytes.
Chem. Biol. Interact. 142(3) , 317-33, (2003) A tyrosinase-directed therapeutic approach for malignant melanoma therapy uses the depigmenting phenolic agents such as 4-hydroxyanisole (4-HA) to form cytotoxic o-quinones. However, renal and hepatic toxicity was reported as side effects in a recent 4-HA cli... |
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Total synthesis of 10-norparvulenone and of O-methylasparvenone using a xanthate-mediated free radical addition-cyclization sequence.
Org. Lett. 5(20) , 3717-9, (2003) [reaction: see text] A short synthesis of (+/-)-10-norparvulenone and (+/-)-O-methylasparvenone was developed starting from commercially available m-methoxyphenol, hinging on a xanthate-mediated addition-cyclization sequence for the construction of the alpha-... |