
CAS Name: Oxo[sulfato(2-)-kO,kO']titanium
Additional Names: titanyl sulfate; titanium sulfate
Percent Composition: O 50.02%, S 20.05%, Ti 29.93%
Literature References: Prepn: E. Hayek, A. Engelbrecht, Monatsh. Chem. 80, 640 (1949). Crystal structure: B. M. Gatehouse et al., Acta Crystallogr. B49, 428 (1993). Catalytic hydrolysis of chlorofluorocarbon: X. Deng et al., J. Catalysis 204, 200 (2001). Prepn of titanium dioxide, q.v.,via thermal hydrolysis: A. V. Tolchev et al., Russ. J. Appl. Chem. 74, 1631 (2001); L. G. Gerasimova et al., ibid. 75, 875 (2002). Sol-gel synthesis of nanosized anatase, a mineral form of titanium dioxide: S. Sivakumar et al., Mater. Lett. 57, 330 (2002). Brief review as whitening agent in tanning: S. Bangaruswamy et al., J. Soc. Leather Technol. Chem. 68, 13-14 (1984).
CAS Name: 2-[(6-Chloro-3-pyridazinyl)thio]-N,N-diethylacetamide
Additional Names: N,N-diethyl-2-[6-(3-chloropyridazinyl)thio]acetamide; N,N-diethyl-2-[6-(3-chloropyridazinyl)mercapto]acetamide;...
Literature References: Prepn: E. Kloimstein et al., Arzneim.-Forsch. 14, 261 (1964); eidem, DE 1188604 (1965 to Lentia). Pharmacology and acute toxicity: H. Stormann, Arzneim.-Forsch. 14, 266 (1964). Toxicology: I. Lindner et al., ibid. 271. Clinical pharmacology: G. Hitzenberger, ibid. 279. Comprehensive description: E. M. Abdel-Moety, H. A. Al-Khamees, Anal. Profiles Drug Subs. 18, 1-32 (1989).
CAS Name: 3,5,5-Trimethyl-2-cyclohexen-1-one
Additional Names: a-isophorone; 1,5,5-trimethyl-3-oxocyclohexene; 1,3,3-trimethylcyclohexen-5-one; isoforon; isoacetophorone
Percent Composition:...
Literature References: Prepn: E. Knoevenagel, Ann. 297, 113 (1897). Synthesis: H. Ueda et al., Agric. Biol. Chem. 30, 1004 (1966); D. S. Torok, W. J. Scott, Tetrahedron Lett. 34, 3067 (1993). Colorimetric field test for determn in air: P. Andrew, R. Wood, Analyst 95, 691 (1970). Solid-phase microextraction/GC determn in aq. samples: J.-Y. Horng, S.-D. Huang, J. Chromatogr. A 678, 313 (1994). Brief description: P. D. Sherman, Jr., A. J. Papa in Kirk-Othmer Encyclopedia of Chemical Technology vol. 13 (Wiley-Interscience, New York, 3rd ed., 1981) pp 918-922. Review of prepn and purification: G. S. Salvapati, M. Janardanarao, J. Sci. Ind. Res. 42, 261-267 (1983). Review of toxicology and human exposure: Toxicological Profile for Isophorone (PB90-180225, 1989) pp 101.
CAS Name: N-[(Cyclohexylamino)carbonyl]-4-[2-(3,4-dihydro-7-methoxy-4,4-dimethyl-1,3-dioxo-2(1H)-isoquinolinyl)ethyl]benzenesulfonamide
Additional Names: 1-cyclohexyl-3-[[p-[2-(3,4-dihydro-7-me...
Literature References: Prepn: E. Kutter et al., DE 2000339 (1971 to Thomae); eidem, US 3708486 (1973 to Boehringer, Ing.); eidem, DE 2011126 (1971 to Thomae), C.A. 76, 14359e (1972). Pharmacokinetics and metabolism: Kopitar, Arzneim.-Forsch. 25, 1455 (1975); Kopitar et al., ibid. 1933.
CAS Name: 9-[(2-Chloro-6-fluorophenyl)methyl]-9H-purin-6-amine
Additional Names: 9-(2-chloro-6-fluorobenzyl)adenineTrademarks: Arpocox (Merck Co.)
Percent Composition: C 51.90%, H 3.27%, Cl...
Literature References: Prepn: E. P. Lira et al., FR 2128600; eidem, US 3846426 (1972, 1974, both to Int. Minerals and Chem.); G. D. Hartman et al., J. Org. Chem. 43, 960 (1978). Determination in feed: D. W. Fink et al., J. Assoc. Off. Anal. Chem. 61, 1078 (1978); 62, 1 (1979). Evaluation of anticoccidial efficacy: P. Schindler et al., Poult. Sci. 58, 23 (1979); L. R. McDougald, J. K. Johnson, ibid. 72.
CAS Name: (16b)-17,21-Dihydroxy-16-methylpregna-1,4-diene-3,11,20-trione
Additional Names: 16b-methylprednisone
Trademarks: Betapred (Schering); Betapar (Parke-Davis); Betalone (Lepetit); De...
Literature References: Prepn: E. P. Oliveto et al., J. Am. Chem. Soc. 80, 4428 (1958); D. Taub et al., ibid. 4435; D. Taub et al., ibid. 82, 4012 (1960); G. G. Nathansohn et al., Experientia 17, 448 (1961); GB 901092 (1962 to Scherico); R. Rausser, E. P. Oliveto, US 3164618 (1965 to Schering).
CAS Name: 2-Bromo-2-nitro-1,3-propanediol
Additional Names: b-bromo-b-nitrotrimethyleneglycol
Trademarks: Bronosol (Green Cross)
Percent Composition: C 18.02%, H 3.02%, Br 39.95%, N 7.00%...
Literature References: Prepn: E. Schmidt, R. Wilkendorf, Ber. 52, 389 (1919); R. Wessendorf, DE 1804068; idem, DE 1954173; idem, US 3658921; idem, US 3711561 (1970, 1971, 1972, 1973 all to Henkel Cie). Antibacterial, antifungal and toxic properties: Z. Eckstein et al., Bull. Acad. Pol. Sci. Ser. Sci. Chim. 11, 687 (1963); B. Croshaw et al., J. Pharm. Pharmacol. 16 (Suppl), 127T (1964); N. G. Clark et al., GB 1057131; eidem, US 3558788 (1967, 1971 both to Boots); R. J. Stretton, T. W. Mason, J. Appl. Bacteriol. 36, 61 (1973). Biotransformation and distribution in rats: H. S. Buttar, R. H. Downie, Toxicol. Lett. 6, 101 (1980). As a nitrosating agent for diethanolamine: I. Schmeltz, A. Wenger, Food Cosmet. Toxicol. 17, 105 (1979); R. L. Elder, J. Environ. Pathol. Toxicol. 4, 47 (1980). Review of bronopol and other preservatives: B. Croshaw, J. Soc. Cosmet. Chem. 28, 3-16 (1977).
CAS Name: 1,2-Dihydro-1,5-dimethyl-4-[(1-methylethyl)amino]-2-phenyl-3H-pyrazol-3-one
Additional Names: 4-isopropylamino-2,3-dimethyl-1-phenyl-3-pyrazolin-5-one; 4-isopropylaminoantipyrine; iso...
Literature References: Prepn: E. Skita, W. Stühmer, DE 930328; DE 932677 (both 1955), C.A. 52, 16372i, 20200h (1958). Acute toxicity: E. Tubaro et al., Arzneim.-Forsch. 20, 1024 (1970). Clinical evaluation of combination with phenylbutazone, q.v., in migraine: W. Sacks, S. Afr. Med. J. 58, 444 (1980).
CAS Name: 2-[4-[2-[(4-Chlorobenzoyl)amino]ethyl]phenoxy]-2-methylpropanoic acid
Additional Names: 2-[p-[2-(p-chlorobenzamido)ethyl]phenoxy]-2-methylpropionic acid; a-[4-(4-chlorobenzoylaminoeth...
Literature References: Prepn: E. Witte et al., DE 2149070; eidem, US 3781328 (both 1973 to Boehringer, Mann.). Pharmacology: R. Zimmerman et al., Atherosclerosis 29, 477 (1978). Clinical studies: A. G. Olsson, P. D. Lang, ibid. 31, 421, 429 (1978); P. Wahl et al., Dtsch. Med. Wochenschr. 103, 1233 (1978). Review of pharmacodynamics and therapeutic use: J. P. Monk, P. A. Todd, Drugs 33, 539-576 (1987).
CAS Name: Carbonic acid diphenyl ester
Additional Names: diphenyl carbonate
Percent Composition: C 72.89%, H 4.71%, O 22.41%
Literature References: Prepn: Eckenroth, Ber. 27, 3410 (1894); Bischoff, ibid. 35, 3434 (1902); Gomberg, Snow, J. Am. Chem. Soc. 47, 198 (1925).
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