biphenol
biphenol structure
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Common Name | biphenol | ||
|---|---|---|---|---|
| CAS Number | 1806-29-7 | Molecular Weight | 186.207 | |
| Density | 1.2±0.1 g/cm3 | Boiling Point | 315.0±0.0 °C at 760 mmHg | |
| Molecular Formula | C12H10O2 | Melting Point | 108-110 °C | |
| MSDS | Chinese USA | Flash Point | 160.8±15.5 °C | |
| Symbol |
GHS05, GHS07 |
Signal Word | Danger | |
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A theoretical investigation on the Strecker reaction catalyzed by a Ti(IV)-complex catalyst generated from a cinchona alkaloid, achiral substituted 2,2'-biphenol, and tetraisopropyl titanate.
Chemistry 19(5) , 1637-46, (2013) The mechanism and the origin of selectivity of the asymmetric Strecker reaction catalyzed by a Ti(IV)-complex catalyst generated from a cinchona alkaloid, achiral substituted 2,2'-biphenol, and tetraisopropyl titanate have been investigated by DFT and ONIOM m... |
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Asymmetric activation of tropos 2,2'-biphenol with cinchonine generates an effective catalyst for the asymmetric strecker reaction of N-tosyl-protected aldimines and ketoimines.
Angew. Chem. Int. Ed. Engl. 46(44) , 8468-70, (2007)
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Facile electrochemical determination of tetrabromobisphenol A based on modified glassy carbon electrode.
Talanta 151 , 209-16, (2016) In this study, surface-functionalized nitrogen-doped graphene was prepared with 1, 3, 6, 8-pyrenetetrasulfonic acid tetrasodium salt in a simple way. The characteristics of the material were demonstrated by UV-vis absorption spectra, X-ray photoelectron spect... |
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Metabolism of 2,2'- and 3,3'-dihydroxybiphenyl by the biphenyl catabolic pathway of Comamonas testosteroni B-356.
Appl. Environ. Microbiol. 70(1) , 174-81, (2004) The purpose of this investigation was to examine the capacity of the biphenyl catabolic enzymes of Comamonas testosteroni B-356 to metabolize dihydroxybiphenyls symmetrically substituted on both rings. Data show that 3,3'-dihydroxybiphenyl is by far the prefe... |
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Degradation of dimeric lignin model compounds by aerobic bacteria isolated from the hindgut of xylophagous termites.
J. Basic Microbiol. 37(3) , 205-11, (1997) The capability of the intestinal flora from the gut of xylophagous termites of degrading lignin model compounds was investigated. Different dimeric lignin model compounds-degrading bacteria were obtained from the hindgut flora of Mastotermes darwiniensis Frog... |
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Antioxidant and cyclooxygenase-2-inhibiting activity of 4,4'-biphenol, 2,2'-biphenol and phenol.
Anticancer Res. 29(6) , 2403-10, (2009) The anthropogenic substance 4,4'-biphenol and its analogues are estrogenic and cytotoxic. It has been previously found that synthesized ortho-dimers of phenolic compounds possess potent antioxidative and anti-inflammatory activity. To clarify the relationship... |
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High energy radiation-induced crosslinking of histone octamer complexes.
Z. Naturforsch., C, J. Biosci. 39(11-12) , 1075-8, (1984) Calf thymus histone octamer complexes were irradiated in the native state in N2O-saturated dilute aqueous solution (0.5 g/l, pH 9, [NaClO4] = 1 -4 mol/l) with 50 or 100 ns pulses of 16 MeV electrons or 60Co-gamma-rays. Time resolved light scattering measureme... |
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Double N-arylation of primary amines: carbazole synthesis from 2,2'-biphenyldiols.
J. Org. Chem. 70(2) , 413-9, (2005) The double N-arylation of primary amines with 2,2'-biphenylylene ditriflates was investigated for the synthesis of multisubstituted carbazoles. Palladium complexes supported by 2-dicyclohexylphosphino-2'-methylbiphenyl or Xantphos [4,5-bis(diphenylphosphino)-... |
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Kinetic evaluation of reactivity of bisphenol A derivatives as radical scavengers for methacrylate polymerization.
Biomaterials 21(21) , 2125-30, (2000) The reactivity of bisphenol A (BPA), diethylstilbestrol (DEST) 2,2'-biphenol (22'BP), 4,4'-biphenol (44'BP) and hydroquinone (HQ) as radical scavengers was examined in 2,2'-azobisisobutyronitrile (AIBN)- and benzoyl peroxide (BPO)-induced methyl methacrylate ... |
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Broad spectrum antimicrobial biocides target the FabI component of fatty acid synthesis.
J. Biol. Chem. 273(46) , 30316-20, (1998) The broad spectrum antibacterial properties of 2-hydroxydiphenyl ethers have been appreciated for decades, and their use in consumer products is rapidly increasing. We identify the enoyl-acyl carrier protein reductase (fabI) component of the type II fatty aci... |