Structure and PMR spectra of isoquercitrin and hirsutrin

Chemistry of Natural Compounds - 1. Two isomers of quercetin 3-glucoside are present in the flowers and leaves of the cotton plant of variety 108-F: hirsutrin, quercetin 3-β-D-glucopyranoside;...     

Use of p-dimethylaminobenzalhyde as a colored reagent for determination of procaine hydrochloride by spectrophotometry

Spectrophotometric determination of procaine hydrochloride is described. The procaine hydrochloride reacts with p-dimethylaminobenzalhyde in glacial acetic acid to form an Schiff base which is a yellow compound, and its maximum absorption wavelength is at 455nm, ₄₅₅=3.46×10⁴. The absorbance for procaine hydrochloride from 0.2 to 15 μg ml⁻¹ obeys Beer's law. The linear regression equation of the calibration graph is C=5.866A−0.02, with a linear regression correlative coefficient is 0.9994 and relative standard deviation (RSD) of 1.7%; the detection limit is 0.1 μg ml⁻¹; recovery is from 92.0 to 110.0%. Effects of reaction medium, temperature, gentamycin, beneylpenicillin, kanamycin, streptomycin, foreign ions, and stand for time on the determination of procaine hydrochloride have been examined. The results obtained by this method agreed with those by the official method (dead-stop titration). This method is rapid and simple, and can be used for the determination of procaine hydrochloride in injection solution of procaine hydrochloride.     

Morestan (6-Methyl-2,3-chinoxalindithiolcarbonat) als Rückstand auf Orangenschalen

Analytical and Bioanalytical Chemistry -     

Reaction of quinoxaline with benzopyridines in acetic anhydrides in the presence of Zn dust

The reaction between quinoxaline and benzopyridine in acetic anhydride in the presence of zinc dust gives a quinoxaline anion and a benzopyridine N-acetyl radical, which recombine to give the previously unknown N-acetyl dihydrobenzo-pyridine derivative of 1,2-dihydroquinoxaline. Under these conditions, quinoxaline alone gives 1,4-diacetyl-1,4-dihydroquinoxaline and 1-acetyl-2-(1,2-dihydroquinoxalyl-2)-1,2-dihydroquinoxaline.Previous communication, [1].Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 967–973, July, 1985.     

Calculated structures of asymmetric modifications of cyanospinels

Structural mechanisms of formation of low-symmetry phases of cyanospinels are described in terms of the phenomenological theory of phase transitions. These are examined for transitions from a spinel structure to two cubic and four rhombohedral phases, induced by automorphic irreducible representations 9-2 and 9-3. Atomic coordinates and the symmetry types of occupied positions in asymmetric phases are determined. Criteria for discrimination between the two as well as between the four phases are formulated. The structures of complex cyanides Tl₂Zn(CN)₄ , K₂Zn(CN)₄, K₂Hg(CN)₄, and Rb₂Hg(CN)₄ are calculated. The displacements and irreducible representations inducing transitions from spinel structures to these phases are determined. Novocherkassk State Technological University. Translated fromZhumal Struktumoi Khimii, Vol. 35, No. 5, pp. 41–49, September–October, 1994. Translated by L. Smolina     

The reaction of chloromethylsilanes with amines,hexamethyldisilazanes, and silylcarhamates

The reactions of chloromethylsilanes with amines, hexamethyldisilazane, and silylcarbamates were studied. The dependence of the composition and structure of the resulting products on the nature of the reagents used and reaction conditions was determined. A scheme for the synthesis of 4,9-diaza-2,7-dioxa-1,6-disilacyclodecane-3,8-dione derivatives was suggested.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 10, pp. 1798–1801, October, 1994.