Peter J. Taormina "Implications of Salt and Sodium Reduction on Microbial Food Safety" in Critical The process of claim 1 wherein the acetic anhydride is present in amounts of 2-3 times by weight of the benzylidene diacetate. The 1 H nuclear magnetic resonance spectral parameters are reported for benzylidene diacetate in CS 2 and acetone-d 6 solutions. Std. Need to identify active compounds in your natural products? It can provide a standard way to encode the molecular information of 2-Benzylidene-1,3-dioxolane to facilitate the search for the compound information in databases and on the web. Catalytic process for the conversion of toluene to equimolar amounts of phenyl acetate and methylene diacetate, Process for making a high octane fuel component, Process to upgrade coal liquids by extraction prior to hydrodenitrogenation. Structure of sodium hydrogen diacetate, redetermined by neutron diffraction" Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry 1975, pp. The analyses were carried out by gas chromatography. Molecular Formula C 26 H 38 Cl 2 N 10 O 4; Average mass 625.550 Da; Monoisotopic mass 624.245483 Da; ChemSpider ID 7838272; More details: Systematic name. Conversion of complicated chemical-related units is no longer sophisticated with the aid of UnitPot. The acetic anhydride should desirably be present in amounts of 2-3 times by weight of the amount of benzylidene diacetate used. Property Name Property Value Reference Molecular Weight 625.5 g/mol Computed by PubChem 2.1 (PubChem release 2019.06.18) Hydrogen Bond Donor Count 8 Computed by Cactvs 126.96.36.199 (PubChem release 2019.06.18) Both phenyl acetate and methylene diacetate are known articles of commerce: the former is a staple article of commerce used as a solvent and as an organic intermediate; the latter material can be used as a high octane fuel component, or as an intermediate in the preparation of formaldehyde. The molecular weight of N-Benzylidene-p-anisidine is available in molecular weight page of N-Benzylidene-p-anisidine, which is calculated as the sum of the atomic weights of each constituent element multiplied by the number of atoms of that element specified in the chemical formula of N-Benzylidene-p-anisidine. © 2020 ChemEssen, Inc. All rights reserved. The process of this invention is conveniently carried out under elevated temperatures of from about 150.degree. to 220.degree. Phenylmethylene diacetate Molecular Formula C 11 H 12 O 4 Average mass 208.211 Da Monoisotopic mass 208.073563 Da ChemSpider ID 21242158 Generally, 0.2 wt.%, is sufficient for this purpose. The N-Benzylidene-p-anisidine molecule contains a total of 29 atom(s). umn class: Standard non-polar; Column diameter: 0.35 mm; Column length: 40 m; Column type: Capillary; Start T: 100 C; CAS no: 581555; Active phase: SE-30; Phase thickness: 0.35 um; Data type: Kovats RI; Authors: Tudor, E., Temperature dependence of the retention index for perfumery compounds on a SE-30 glass capillary column. Benzylidene diacetate may be converted to phenyl acetate and methylene diacetate by an acid-catalyzed reaction in the presence of oxygen or air, and acetic anhydride, at elevated temperatures and pressures. One method for preparing the benzylidene diacetate starting material is by the acid catalyzed reaction of benzaldehyde with acetic anhydride disclosed in J.A.C.S., 72, 847 (1950). Thus, each side of the chemical equation must represent the same quantity of any particular element based on the chemical formula. The molecular weight of 2-Benzylidene-1,3-dioxolane is available in molecular weight page of 2-Benzylidene-1,3-dioxolane, which is calculated as the sum of the atomic weights of each constituent element multiplied by the number of atoms of that element specified in the chemical formula of 2-Benzylidene-1,3-dioxolane. The chemical formula of 2-Benzylidene-1,3-dioxolane shown above is based on the molecular formula indicating the numbers of each type of atom in a molecule without structural information, which is different from the empirical formula which provides the numerical proportions of atoms of each type. In organic chemistry, a benzylidene acetal is the functional group with the structural formula C 6 H 5 CH(OR) 2 (R = alkyl, aryl). 4 The above chemical formula is the basis of stoichiometry in chemical equations, i.e., the calculation of relative quantities of reactants and products in chemical reactions. 5. An alternative textual expression including the structural information is InChI. éiConvertFormula\bhj, VBS t@CT[oÌtH_ÌLqû@ÉÂ¢Ä, EXCEL©çCSVt@CðACCSESSÉÇÁEÒWðs¢½¢, t@CgpÌtH_¼ÒWsÂh~û@, I[g[VG[ñðµ½¢iYtoceÜÈãÉÈéÆG[j. C., preferably 200.degree. Benzylidene acetals are used as protecting groups in glycochemistry. Heat of Vaporization at Normal Boiling Point, LogP (Octanol-Water Partition Coefficient), Ghose-Crippen Octanol-Water Partition Coefficient (logP), Moriguchi Octanol-Water Partition Coefficient (logP), Activity Score for Ion Channel Modulators, Activity Score for Nuclear Receptor Ligands, Structure Data File (SDF/MOL File) of N-Benzylidene-p-anisidine, download in the SDF page of N-Benzylidene-p-anisidine, Chemical structure of N-Benzylidene-p-anisidine, chemical structure page of N-Benzylidene-p-anisidine, Molecular weight of N-Benzylidene-p-anisidine, molecular weight page of N-Benzylidene-p-anisidine, (NE)-4-methoxy-N-(phenylmethylidene)aniline, 29 atom(s) - 13 Hydrogen atom(s), 14 Carbon atom(s), 1 Nitrogen atom(s) and 1 Oxygen atom(s), 30 bond(s) - 17 non-H bond(s), 13 multiple bond(s), 3 rotatable bond(s), 1 double bond(s), 12 aromatic bond(s), 2 six-membered ring(s), 1 imine(s) (aromatic) and 1 ether(s) (aromatic), 1-((1E)-2-phenyl-1-azavinyl)-4-methoxybenzene, 4-methoxy-N-[(Z)-phenylmethylidene]aniline, 4-Methoxy-N-[(E)-phenylmethylidene]aniline, Benzenamine, 4-methoxy-N-(phenylmethylene)-, (E)-, Benzenamine, 4-methoxy-N-(phenylmethylene)-.
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