
CAS Name: 1,2,3,5,6,7-Hexahydroxy-9,10-anthracenedione
Additional Names: 1,2,3,5,6,7-hexahydroxyanthraquinone; rufigallic acid; C.I. 58600
Percent Composition: C 55.27%, H 2.65%, O 42.07%
Literature References: Prepd by the action of H2SO4 on gallic acid: Robiquet, Ann. 19, 204 (1836); by dry distn of gallic acid: Kunz-Krause, Manicke, Ber. 53, 190 (1920). See also: Colour Index vol. 4 (3rd ed., 1971) p 4520.
CAS Name: 1-Bromododecane
Additional Names: dodecyl bromide
Percent Composition: C 57.83%, H 10.11%, Br 32.06%
Literature References: Prepd by the action of hydrobromic acid on primary n-lauryl alcohol in the presence of sulfuric acid: Kamm, Marvel, Org. Synth. 1, 7 (1921).
CAS Name: 1,3-Dibromopropane
Additional Names: a,g-dibromopropane; w,w'-dibromopropane; trimethylene dibromide
Percent Composition: C 17.85%, H 3.00%, Br 79.16%
Literature References: Prepd by the action of hydrobromic acid on trimethylene glycol in the presence of sulfuric acid: Kamm, Marvel, Org. Synth. coll. vol. I, p 30 (1941); cf. Derick, Hess, J. Am. Chem. Soc. 40, 545 (1918); Norris, Mulliken, ibid. 42, 2096 (1920): Kamm, Newcomb, ibid. 43, 2229 (1921). From trimethylene glycol and PBr3: Bogert, Slocum, ibid. 46, 765 (1924).
CAS Name: (Trifluoromethyl)benzene
Additional Names: a,a,a-trifluorotoluene; phenylfluoroform
Percent Composition: C 57.54%, H 3.45%, F 39.01%
Literature References: Prepd by the action of hydrogen fluoride on benzotrichloride: Simons, Lewis, J. Am. Chem. Soc. 60, 492 (1938); Simons, Ind. Eng. Chem. 32, 178 (1940); by the action of antimony trifluoride on benzotrichloride: Swarts, Bull. Sci. Acad. R. Belg., [4] 35, 375 (1898); [5] 6, 389 (1920); [5] 13, 175 (1927); Holt et al., US 2058453 (1937 to Kinetic Chemicals).
CAS Name: 5,7-Diiodo-8-quinolinol
Additional Names: diiodohydroxyquin; diiodo-oxyquinoline; 5,7-diiodo-8-hydroxyquinolineTrademarks: Diodoquin (Searle); Disoquin; Floraquin (Searle); Dyodin; Di...
Literature References: Prepd by the action of iodine monochloride on 8-hydroxyquinoline: Papesch, Burtner, J. Am. Chem. Soc. 58, 1314 (1936); by the action of KIO3 on 8-hydroxyquinoline: Zeifman, C.A. 34, 3745. Electrolytic prepn: Brown, Berkowitz, Trans. Electrochem. Soc. 75, 385 (1939). See also Claus, DE 78880; Passek, DE 411050; Matsumura, C.A. 21, 1461 (1927); Pirrone, Cherubino, C.A. 28, 3073 (1934).
CAS Name: Tetraiodoethene
Additional Names: diiodoform; ethylene periodide; ethylene tetraiodide
Percent Composition: C 4.52%, I 95.48%
Literature References: Prepd by the action of iodine on diodoacetylene obtained from calcium carbide and iodine. Crystal and molecular structure: B. C. Haywood, R. Shirley, Acta Crystallogr. B33, 1765 (1977).
Additional Names: b-Aminopropionic acid; 3-aminopropanoic acid; 3-aminopropionic acid
Trademarks: Abufène (Thaplix)
Percent Composition: C 40.44%, H 7.92%, N 15.72%, O 35.92%
Literature References: Prepd by the action of KOBr and KOH upon succinimide: Clarke, Behr, Org. Synth. 16, 1 (1936). By the action of liq ammonia upon methyl acrylate: Morsch, Monatsh. Chem. 63, 220 (1933), cf. C.A. 41, 4104 (1947); by the addition of NH4OH to acrylonitrile: Ford et al., J. Am. Chem. Soc. 69, 844 (1947). By electrolytic oxidation of 3-amino-1-propanol in H2SO4 using Pb electrodes without diaphragm: Jubilee Vol. Emil Barell 1946, 85-91. For industrial methods of prepn see several pats. by T. L. Gresham to B. F. Goodrich. Prepn from ethylene cyanohydrin (b-hydroxypropionitrile): Boatright, US 2734081 (1956 to Am. Cyanamid); from b-aminopropionitrile: Ford, Org. Synth. coll. vol. III, 34 (1955). Improved process: Beutel, Klemchuk, US 2956080 (1960 to Merck Co.).
Additional Names: Magnesium diethyl
Percent Composition: C 58.28%, H 12.23%, Mg 29.49%
Literature References: Prepd by the action of magnesium metal on mercury diethyl in ether: Schlenk, Jr., Ber. 64, 734, 736 (1931).
Additional Names: Magnesium diphenyl
Percent Composition: C 80.74%, H 5.65%, Mg 13.62%
Literature References: Prepd by the action of magnesium on mercury diphenyl: Schlenk, Jr., Ber. 64, 736 (1931); Gilman, Brown, Rec. Trav. Chim. 49, 202 (1930).
CAS Name: Carbon selenide
Percent Composition: C 7.07%, Se 92.93%
Literature References: Prepd by the action of methylene chloride vapor on heated selenium: Ives et al., J. Chem. Soc. 1947, 1080; or from a mixture of CCl4 and H2Se in a stream of N2 at 500°: Grimm, Metzger, Ber. 69, 1356 (1936); from the elements by electrical discharge on Se vapor in the presence of sugar charcoal: Steudel, Z. Anorg. Allg. Chem. 361, 195 (1968).
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