192996
α-Methyl-2-naphthalenemethanol
98%
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About This Item
Produits recommandés
Pureté
98%
Forme
solid
Pf
73-78 °C (lit.)
Chaîne SMILES
CC(O)c1ccc2ccccc2c1
InChI
1S/C12H12O/c1-9(13)11-7-6-10-4-2-3-5-12(10)8-11/h2-9,13H,1H3
Clé InChI
AXRKCRWZRKETCK-UHFFFAOYSA-N
Description générale
α-Methyl-2-naphthalenemethanol forms complexes and multimers with methyl lactate. α-Methyl-2-naphthalenemethanol on reaction with sulfur trioxide-dimethylformamide complex and pyridine yields sulfated products.
Code de la classe de stockage
11 - Combustible Solids
Classe de danger pour l'eau (WGK)
WGK 3
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
Équipement de protection individuelle
Eyeshields, Gloves, type N95 (US)
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Identification of sulfation sites of metabolites and prediction of the compounds' biological effects.
Analytical and Bioanalytical Chemistry, 383(6), 666-674 (2006)
Journal of chemical theory and computation, 13(5), 2230-2244 (2017-04-19)
We introduce a novel method, Pathway Search guided by Internal Motions (PSIM), that efficiently finds molecular dissociation pathways of a ligand-receptor system with guidance from principal component (PC) modes obtained from molecular dynamics (MD) simulations. Modeling ligand-receptor dissociation pathways can
Physical chemistry chemical physics : PCCP, 11(35), 7589-7598 (2009-12-03)
Complexation between (1R,2S)-(+)-cis-1-amino-2-indanol (AI) and the two enantiomers of methyl lactate has been studied by means of laser-induced fluorescence, resonance-enhanced two-photon ionisation, and IR-UV double resonance spectroscopy, in the region of 3 microm. Two isomeric complexes have been spectroscopically characterised
Journal of chromatography. A, 1599, 144-151 (2019-04-21)
Coated-type chiral stationary phases (CSPs) for high-performance liquid chromatography (HPLC) were prepared from three cyclic amylose tris(3,5-dimethylphenylcarbamate) (cADMPC) samples, of which weight-average molar mass (Mw) ranges from 19 to 91 kg mol-1, and from three linear ADMPC samples ranging in Mw
Chemico-biological interactions, 315, 108905-108905 (2019-11-26)
Mineral oils are widely applied in food production and processing and may contain polycyclic aromatic hydrocarbons (PAHs). The PAHs that may be present in mineral oils are typically alkylated, and have been barely studied. Metabolic oxidation of the aromatic ring
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