
CAS Name: 2-Propanol aluminum salt
Additional Names: aluminum isopropylate
Percent Composition: C 52.93%, H 10.36%, Al 13.21%, O 23.50%
Literature References: Prepd from aluminum and isopropyl alcohol in the presence of mercuric chloride: Young et al., J. Am. Chem. Soc. 58, 100 (1936); by adding excess isopropyl alcohol to a benzene soln of AlCl3 at 6°: Teichner, Compt. Rend. 237, 810 (1953). Forms trimers and tetramers: Shiner et al., J. Am. Chem. Soc. 85, 2318 (1963); Oliver et al., J. Inorg. Nucl. Chem. 31, 1609 (1969); Worrall, J. Chem. Educ. 46, 510 (1969). Toxicity: Smyth et al., Am. Ind. Hyg. Assoc. J. 30, 470 (1969). Review: Whitaker in Adv. Chem. Ser. 23, entitled "Metal-Organic Compounds," M. Sittig, Ed. (ACS, Washington DC, 1959) pp 184-189.
CAS Name: Bis(aceto-kO)hydroxyaluminum
Additional Names: hydroxybis(acetato)aluminum; basic aluminum acetate; aluminum diacetate; aluminum subacetate; aluminum hydroxyacetate
Trademarks: Len...
Literature References: Prepd from aluminum hydroxide and acetic acid or from sodium acetate and aluminum chloride hexahydrate: Hood, Ihde, J. Am. Chem. Soc. 72, 2094 (1950). Other methods of prepn: Gmelins, Aluminum (8th ed.) 35B, p 296 (1934). Also prepd in aq solution, see Aluminum Subacetate Solution.
CAS Name: 2-Methyl-2-propanol aluminum salt
Percent Composition: C 58.51%, H 11.05%, Al 10.95%, O 19.49%
Literature References: Prepd from aluminum tert-butyl alcohol and mercuric chloride: Wayne, Adkins, Org. Synth. coll. vol. III, 48 (1955).
CAS Name: (Dimethylamino)oxoacetic acid 2-acetyl-2-methyl-1-phenylhydrazide
Additional Names: 1-acetyl-1,5,5-trimethyl-2-phenylsemioxamazide; a-(dimethylamidooxalyl)-b,b-methylacetylphenylhydra...
Literature References: Prepd from aminopyrine by oxidation with 30% hydrogen peroxide: Charonnat, Delaby, Compt. Rend. 189, 850 (1929); Valyashko, Depeshko, Zh. Obshch. Khim. 20, 1667 (1950).
CAS Name: Isothiocyanatobenzene
Additional Names: isothiocyanic acid phenyl ester; phenyl mustard oil; thiocarbanil
Percent Composition: C 62.19%, H 3.73%, N 10.36%, S 23.72%
Literature References: Prepd from ammonium phenyldithiocarbamate by the action of lead nitrate: Dains et al., Org. Synth. coll. vol. I (2nd ed., 1941) p 447.
Additional Names: Ammonium bichromate
Percent Composition: Cr 41.26%, H 3.20%, N 11.11%, O 44.43%
Literature References: Prepd from ammonium sulfate and sodium dichromate or by the interaction of ammonia gas and chromic acid in soln: Hartford, Ind. Eng. Chem. 41, 1993 (1949); Chromium Chemicals Vol. 52 (Mutual Chem. Div., Allied Chem.) p. 34-39. Review: ACS Monograph Series no. 132, entitled "Chromium," vol. 1, M. J. Udy, Ed. (Reinhold, New York, 1956) passim.
CAS Name: 3,3-Bis(4-hydroxyphenyl)-1(3H)-isobenzofuranone disodium salt
Percent Composition: C 66.30%, H 3.34%, Na 12.69%, O 17.66%
Literature References: Prepd from an alcoholic soln of 1 mol phenolphthalein by the addition of 2 mols NaOH. Structure: Buu-Hoi, Bull. Soc. Chim. [5] 8, 165 (1941).
CAS Name: 4,5-Dihydro-2-[[5-methyl-2-(1-methylethyl)phenoxy]methyl]-1H-imidazole
Additional Names: 2-[(thymyloxy)methyl]-2-imidazoline; 2-(thymyloxymethyl)glyoxalidine; 2-[(p-mentha-1,3,5-trien...
Literature References: Prepd from an alkyl thymyloxyacetimidate and ethylenediamine: Sonn, US 2149473 (1939 to Ciba); Djerassi, Scholz, J. Am. Chem. Soc. 69, 1688 (1947). Pharmacology: Pham-Huu-Chanh et al., Therapie 24, 797 (1969).
CAS Name: 1,2-O-[(1R)-2,2,2-Trichloroethylidene]-a-D-glucofuranose
Additional Names: a-D-glucochloralose; glucochloral; anhydroglucochloral; chloralosane
Trademarks: Alphakil (Rentokil); Dor...
Literature References: Prepd from anhydr glucose and trichloroacetaldehyde (anhydr chloral); b-chloralose is also formed. Prepn: M. Hanroit, C. Richet, C.R. Hebd. Seances Acad. Sci. 116, 63 (1893); and structure: Pictet, Reichel, Helv. Chim. Acta 6, 621 (1923); Freudenberg, Vajda, J. Am. Chem. Soc. 59, 1955 (1937); cf. Coles et al., ibid. 51, 519 (1929); White, Hixon, ibid. 55, 2438 (1933). Crystal structure: T. Taga et al., Acta Crystallogr. B38, 1874 (1982). Immobilizing agent in control of depredating birds: Redpath et al., Ann. Appl. Biol. 49, 77 (1961). Anesthetic for dogs in experimental work: B. G. Bass, N. M. Buckley, Am. J. Physiol. 210, 854 (1966); R. H. Cox, ibid. 223, 660 (1972). CNS depressant activity: J. L. Barker, Nature 252, 52 (1974). GLC determn in rodenticides: J. Theobald, J. Chromatogr. 129, 444 (1976); in tissue: E. Odam et al., Analyst 109, 1335 (1984). Acute toxicity: E. W. Schafer, Toxicol. Appl. Pharmacol. 21, 315 (1972). Review of pharmacology: G. U. Balis, R. R. Monroe, Psychopharmacologia 6, 1-30 (1964); and toxicology: P. Lees, Vet. Rec. 91, 330-333 (1972). Review as canine anesthetic: H. Holzgrefe et al., Lab. Anim. Sci. 37, 587-595 (1987).
Additional Names: Anilinoacetic acid
Percent Composition: C 63.57%, H 6.00%, N 9.27%, O 21.17%
Literature References: Prepd from aniline and chloroacetic acid: Curtius, J. Prakt. Chem. 38, 436 (1888); Thorpe, Wood, J. Chem. Soc. 103, 1606 (1913).
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