
CAS Name: Diphenylethanedione
Additional Names: bibenzoyl; dibenzoyl; diphenylglyoxal; diphenyl-a,b-diketone
Percent Composition: C 79.98%, H 4.79%, O 15.22%
Literature References: Prepd by the oxidation of benzoin, C6H5CH(OH)COC6H5, with HNO3 or with a copper sulfate-pyridine mixture: Adams, Marvel, Org. Synth. vol. I, p 25 (1921); Clarke, Dreger, ibid. coll. vol. I, 80 (87, 2nd ed); Hatt et al., J. Chem. Soc. 1936, 93; L. F. Fieser, Experiments in Organic Chemistry (Boston, 3rd ed, 1955) p 173; Organic Experiments (Boston, 1964) p 214.
CAS Name: 5,6,7,8-Tetrahydro-4-methoxy-6-methyl-1,3-dioxolo[4,5-g]isoquinolin-5-ol
Percent Composition: C 60.75%, H 6.37%, N 5.90%, O 26.97%
Literature References: Prepd by the oxidation of narcotine with dil nitric acid. Synthesis: Salway, J. Chem. Soc. 97, 1208 (1910). Is tautomeric. Structure studies: Small, Lutz, "Chemistry of the Opium Alkaloids," Supplement No. 103, U.S. Public Health Reports (Washington, 1932) p 49; Schneider, Müller, Ann. 615, 34 (1958). Absorption spectrum: Csokán, Z. Anal. Chem. 124, 344 (1942).
Additional Names: Disodium dihydrogen subphosphate; sodium dihydrogen hypophosphate; sodium acid hypophosphate
Percent Composition: H 0.98%, Na 22.33%, O 46.61%, P 30.08%
Literature References: Prepd by the oxidation of red phosphorus with sodium chlorite in water: Leininger, Chulski, Inorg. Synth. 4, 68 (1953).
CAS Name: [Carbonato(1-)-O]dihydroxyaluminum monosodium salt
Additional Names: aluminum sodium carbonate hydroxide
Trademarks: Kompensan (Roerig); Minicid
Percent Composition: C 8.34%, H ...
Literature References: Prepd by the reaction between an aluminum alkoxide and NaHCO3 in water: Grote, US 2783179 (1957 to Chattanooga Medicine).
CAS Name: 5-Hydroxy-4-octanone
Additional Names: 5-octanol-4-one
Percent Composition: C 66.63%, H 11.18%, O 22.19%
Literature References: Prepd by the reaction between an ether soln of ethyl butyrate and sodium or potassium: Bouveault, Locquin, Bull. Soc. Chim. [3] 35, 629 (1906); Corson et al., J. Am. Chem. Soc. 52, 3988 (1930); Scheibler, Emden, Ann. 434, 265 (1923); Snell, McElvain, Org. Synth. coll. vol. II, 114 (1943).
CAS Name: 1-[[2-(Diethylamino)ethyl]amino]-4-methyl-9H-thioxanthen-9-one hydrochloride
Additional Names: 1-(2-diethylaminoethylamino)-4-methylthiaxanthone hydrochlorideTrademarks: Miracil D; Ni...
Literature References: Prepd by the reaction of 1-chloro-4-methylthiaxanthone with asym-diethylethylenediamine: Mauss, Naturwissenschaften 33, 253 (1946); idem, Ber. 81, 19 (1948); Sharp, J. Chem. Soc. 1951, 2961; Archer, Suter, J. Am. Chem. Soc. 74, 4296 (1952). Review of mode of action: Weinstein, Hirschberg, Prog. Mol. Subcell. Biol. 2, 232 (1971). Review: Hirschberg in Antibiotics vol. 3, J. W. Corcoran, F. E. Hahn, Eds. (Springer-Verlag, New York, 1975) pp 274-303.
CAS Name: N,N,N-Trimethyl-1,3-dioxolane-4-methanaminium iodide
Additional Names: (1,3-dioxolan-4-ylmethyl)trimethylammonium iodide; 4-(dimethylaminomethyl)-1,3-dioxacyclopentane methiodide; 1-d...
Literature References: Prepd by the reaction of a cyclic acetal of an a-monohalohydrin of glycerol with dimethylamine which on treatment with methyl iodide results in a quaternary ammonium salt: Fourneau, US 2445393 (1948 to Rhône-Poulenc).
CAS Name: Bis(phenylmethyl) disulfide
Additional Names: benzyl disulfide; a-(benzyldithio)toluene; di(phenylmethyl)disulfide
Percent Composition: C 68.25%, H 5.73%, S 26.03%
Literature References: Prepd by the reaction of benzyl chloride with sodium disulfide or polysulfide: Blanksma, Rec. Trav. Chim. 20, 137 (1901); Moran, Crandall, US 2113092 (1938); Wojcik, US 2185007 (1939).
Percent Composition: C 35.25%, H 8.87%, O 18.78%, Si 37.09%
Literature References: Prepd by the reaction of hexamethyldisiloxane with octamethylcyclotetrasiloxane and sulfuric acid; by varying the proportions of these reactants, other methylpolysiloxanes of a desired average molecular weight may be prepd: Patnode, Wilcock, J. Am. Chem. Soc. 68, 362 (1946).
Percent Composition: Cl 21.69%, H 0.62%, O 29.37%, Se 48.32%
Literature References: Prepd by the reaction of hydrogen chloride and selenium trioxide: Le Geyt et al., J. Chem. Soc. 123, 2870 (1923).
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