
Percent Composition: C 16.15%, H 1.36%, Ni 39.46%, O 43.03%
Literature References: Prepd by reaction of formic acid with Ni: Johnson, US 2576072 (1951 to Harshaw Chemical); with NiCO3: Bircumshaw, Edwards, J. Chem. Soc. 1950, 1800.
CAS Name: Tetracosamethylundecasiloxane
Percent Composition: C 34.74%, H 8.75%, O 19.28%, Si 37.23%
Literature References: Prepd by reaction of hexamethyldisiloxane with octamethylcyclotetrasiloxane and sulfuric acid: Patnode, Wilcock, J. Am. Chem. Soc. 68, 362 (1946); by cohydrolysis of ethoxytrimethylsilane and diethoxydimethylsilane: Hyde, US 2457677 (1948 to Corning Glass).
CAS Name: 4,4'-[1,3-Phenylenebis(azo)]bis[1,3-benzenediamine] dihydrochloride
Additional Names: C.I. Basic Brown 1; 4,4'-[m-phenylenebis(azo)]bis[m-phenylenediamine] dihydrochloride; C.I. 21000...
Literature References: Prepd by reaction of m-phenylenediamine HCl and nitrous acid: F. J. Welcher, Organic Analytical Reagents (D. Van Nostrand Co., New York, 1948) p 339; Colour Index vol. 4 (3rd ed., 1971) p 4154.
CAS Name: Phosphoric acid tributyl ester
Percent Composition: C 54.12%, H 10.22%, O 24.03%, P 11.63%
Literature References: Prepd by reaction of POCl3 with butyl alcohol: Pianfetti, Janey, US 3020303 (1962 to FMC). Toxicity study: Smyth, Carpenter, J. Ind. Hyg. Toxicol. 26, 269 (1944).
CAS Name: 1,2-Dibromoethene
Additional Names: 1,2-dibromoethylene; sym-dibromoethylene
Percent Composition: C 12.93%, H 1.08%, Br 85.99%
Literature References: Prepd by reaction of tetrabromoethylene with Zn and alc followed by sepn of cis- and trans-forms by fractional distillation: Noyes et al., J. Am. Chem. Soc. 72, 33 (1950).
CAS Name: endo-8-Methyl-8-azabicyclo[3.2.1]octan-3-ol
Additional Names: 1aH,5aH-tropan-3a-ol; 2,3-dihydro-3a-hydroxy-8-methylnortropidine; 2,3-dihydro-3a-hydroxytropidine
Percent Composition...
Literature References: Prepd by reaction of tropidine and HBr, followed by hydrolysis and separation of isomers, tropine and pseudotropine: Ladenburg, Ber. 35, 1159 (1902); by hydrogenation of tropinone in the presence of Raney nickel: Van de Kamp, Sletzinger, US 2366760 (1945 to Merck Co.); Stoll et al., US 2746976 (1956 to Sandoz). Yield of tropine and pseudotropine under varying conditions of reduction: Beckett et al., Tetrahedron 6, 319 (1959). Separation of tropine and pseudotropine by gold salt formation: Ladenburg, loc. cit.; by fractional distillation under reduced pressure: Friess et al., Toxicol. Appl. Pharmacol. 2, 574 (1960). Stereochemistry: Beyerman et al., Rec. Trav. Chim. 75, 1445 (1956).
CAS Name: a-Phenylbenzenemethanol
Additional Names: benzhydrol; diphenylcarbinol
Percent Composition: C 84.75%, H 6.57%, O 8.68%
Literature References: Prepd by reducing benzophenone with zinc dust in strongly alkaline soln: Wiselogle, Sonneborn, Org. Synth. coll. vol. I (2nd ed, 1941) p 90. By reducing benzophenone with magnesium in methanol: Zechmeister, Rom, Ann. 468, 123 (1929).
Additional Names: 2,3-Benzodiazine; benzo[d]pyridazine; b-phenodiazine
Percent Composition: C 73.83%, H 4.65%, N 21.52%
Literature References: Prepd by reduction of 1-chlorophthalazine with hydriodic acid and red phosphorus: Gabriel, Eschenbach, Ber. 30, 3024 (1897); Paul, Ber. 32, 2015 (1899); by redn of 1-hydrazinophthalazine: Armarego, J. Appl. Chem. 11, 70 (1961); from o-phthalaldehyde + hydrazine sulfate: Smith, Otremba, J. Org. Chem. 27, 879 (1962); from 1,2-benzodinitrile: Carter, Cheeseman, Org. Prep. Proced. Int. 6, 67 (1974).
CAS Name: 4-Methoxybenzenemethanol
Additional Names: p-methoxybenzyl alcohol; anisyl alcohol
Percent Composition: C 69.55%, H 7.30%, O 23.16%
Literature References: Prepd by reduction of anisaldehyde with triisobutyl aluminum and with amine boranes: Ziegler et al., Ann. 623, 9 (1959); Chamberlain, Schechter, US 2898379 (1959 to Callery Chemical). Toxicity study: Woodart et al., J. Pharmacol. Exp. Ther. 93, 26 (1948).
CAS Name: 5b-Pregnane
Additional Names: 17b-ethyletiocholane
Percent Composition: C 87.42%, H 12.58%
Literature References: Prepd by reduction of etiocholyl methyl ketone or of pregnanedione: Butenandt, Ber. 64, 2529 (1931); Marker et al., J. Am. Chem. Soc. 60, 1067 (1938); Steiger, Reichstein, Helv. Chim. Acta 21, 161 (1938).
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