
CAS Name: a-[(Dimethylamino)methyl]-3,4-dimethoxybenzenemethanol
Additional Names: a-[(dimethylamino)methyl]veratryl alcohol; 3,4-dimethoxy-a-[(dimethylamino)methyl]benzyl alcohol; dimethylamin...
Literature References: Prepn of dl-form: La Manna et al., Farmaco Ed. Sci. 15, 9 (1960); Chapman et al., Proc. R. Soc. London Ser. B 163, (990), 116 (1965); Hodgkins et al., Tetrahedron Lett. 1967, 1321; of d- and l-forms: La Manna et al., loc. cit. Isoln of l-form from cactus, Coryphantha macromeris (Engelm.) Lem., Britton and Rose, Cactaceae: Hodgkins et al., loc. cit.
CAS Name: 2-Bromo-3-methylbutanoic acid
Percent Composition: C 33.17%, H 5.01%, Br 44.14%, O 17.68%
Literature References: Prepn of dl-form: Ley, Popow, Ann. 174, 61 (1874); Smissman, J. Am. Chem. Soc. 76, 5805 (1954); Marvel, Org. Synth. coll. vol. III, 848 (1955). Prepn of d- and l-forms: Berlingozzi, Furia, Gazz. Chim. Ital. 56, 82 (1926); Berlingozzi, Lenoci, ibid. 68, 721 (1938). Configuration of d-form: Brewster et al., Nature 166, 179 (1950).
CAS Name: 2-(2,2-Diphenyl-1,3-dioxolan-4-yl)piperidine
Additional Names: 2,2-diphenyl-4-(2-piperidyl)-1,3-dioxolane
Percent Composition: C 77.64%, H 7.49%, N 4.53%, O 10.34%
Literature References: Prepn of dl-forms and resolution of a-racemates: Hardie, Halverstadt, BE 613262; US 3262938 (1962, 1966 both to Cutter Labs.); W. R. Hardie et al., J. Med. Chem. 9, 127 (1966).
CAS Name: [4S-(4a,4aa,5a,5aa,6a,12aa)]-4-(Dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,5,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-2-naphthacenecarboxamide monohydrate
Additional Names: a-6...
Literature References: Prepn of family of 6-deoxytetracyclines: C. R. Stephens et al., J. Am. Chem. Soc. 80, 5324 (1958). See also: McCormick, Jensen, US 3019260 (1962 to Am. Cyanamid). Prepn, separation and configuration of 6a- and 6b-epimers: M. S. von Wittenau et al., J. Am. Chem. Soc. 84, 2645 (1962); C. R. Stephens et al., ibid. 85, 2643 (1963). Prepn of 6a-deoxyoxytetracycline: R. K. Blackwood et al., US 3200149 (1965 to Pfizer). 1H-NMR study: M. S. von Wittenau, R. K. Blackwood, J. Org. Chem. 31, 613 (1966). Biological properties: English, Proc. Soc. Exp. Biol. Med. 122, 1107 (1966). Pharmacology: Fabre, Chemotherapia 11, 73 (1966); Gibaldi, ibid. 12, 265 (1967). Toxicity of hyclate: Goldenthal, Toxicol. Appl. Pharmacol. 18, 185 (1971). Clinical trial in prophylaxis of leptospirosis: E. T. Takafuji et al., N. Engl. J. Med. 310, 497 (1984). Clinical trial in periodontitis: A. M. Polson et al., J. Periodontol. 68, 110, 119 (1997). Review: C. Edwards in Pharmacological and Biochemical Properties of Drug Substances vol. 2, M. E. Goldberg, Ed. (Am. Pharm. Assoc., Washington, DC, 1979) pp 305-332.
CAS Name: [4-(Acetylamino)phenyl]arsonic acid
Additional Names: p-acetamidobenzenearsonic acid; N-acetyl-p-aminobenzenearsonic acid; N-acetylarsanilic acid
Percent Composition: C 37.09%, H 3...
Literature References: Prepn of free acid and sodium salt: Bart, Ann. 429, 55 (1922). Toxicity: A. Gros, Biochem. Z. 184, 360 (1927).
CAS Name: (1b,2b)-6-Chloro-1,2-dihydro-17-hydroxy-3'H-cyclopropa[1,2]pregna-1,4,6-triene-3,20-dione
Additional Names: 6-chloro-17-hydroxy-1a,2a-methylenepregna-4,6-diene-3,20-dione; 6-chloro-6-...
Literature References: Prepn of free alcohol: Wiechert, Neumann, DE 1189991 C.A. 63, 1842e (1965); Wiechert, US 3234093 (1965, 1966 both to Schering AG). Biodynamics in man: Gerhards et al., Arzneim.-Forsch. 23, 1550 (1973). The free alcohol is an anti-androgen; the acetate is both an anti-androgen and a progestogen. Effect on hormone secretion and on spermatogenesis in man: L. Moltz et al., Contraception 21, 393 (1980). Review of pharmacology and clinical studies (acetate) on acne and hirsutism in women: J. Hammerstein et al., J. Steroid Biochem. 19, 591 (1983).
Percent Composition: Al 18.14%, Sb 81.86%
Literature References: Prepn of high purity crystals, resistance measurements, activation energies: Justi, Lautz, Abh. Braunschw. Wiss. Ges. 5, 36 (1953); C.A. 48, 1756i (1954). Electrical properties: Willardson et al., J. Electrochem. Soc. 101, 354 (1954); and prepn: Kover, Compt. Rend. 243, 648 (1956). Zone melting to remove impurities and to improve electr properties: Scheel, Z. Metallkd. 46, 58 (1955), C.A. 49, 4486f (1955). Oxidation by water: Rudorff, Kohlmeyer, Z. Metallkd. 45, 608 (1954), C.A. 49, 7432c (1955).
CAS Name: 3-Ethyl-6,7-dimethoxy-1-(phenylmethyl)isoquinoline
Additional Names: 1-benzyl-3-ethyl-6,7-dimethoxyisoquinoline
Percent Composition: C 78.15%, H 6.89%, N 4.56%, O 10.41%
Literature References: Prepn of hydrochloride: FR 1362765 (1964 to Orgamol, SA), C.A. 62, 536f (1965). Physical properties and solution stability: E. Pawelczyk, M. Zajac, Diss. Pharm. Pharmacol. 24, 5 (1972). HPLC determn in pharmaceutical formulations: E. H. Girgis, J. Pharm. Sci. 82, 503 (1993).
CAS Name: 1-(1,3-Benzodioxol-5-ylmethyl)-4-[(4-chlorophenoxy)acetyl]piperazine
Additional Names: 1-[(p-chlorophenoxy)acetyl]-4-piperonylpiperazine; 1-[2-(4-chlorophenoxy)acetyl]-4-(3,4-methylen...
Literature References: Prepn of hydrochloride: A. Buzas, R. Pierre, FR M7524 (1970 to Lab Bouchard), C.A. 75, 112865r (1971). Manufacturing process: G. P. Gardini et al., US 4225714 (1980 to Farmaceutici Geymon.). Improved prepn: G. P. Gardini et al., Synth. Commun. 12, 887 (1982). Determn by TLC: G. Musumarra et al., J. Chromatogr. 350, 151 (1985). Toxicology and pharmacology: G. David et al., Acta Ther. 11, 387 (1985). Clinical trial in the elderly: B. Bompani, G. Scali, Curr. Med. Res. Opin. 10, 99 (1986).
CAS Name: 2-Hydroxy-2,6,6-trimethylbicyclo[3.1.1]heptan-3-one
Additional Names: 2-hydroxy-3-pinanone; 2-hydroxypinocamphone
Trademarks: Camphostene; Oxypinone
Percent Composition: C 71.39...
Literature References: Prepn of l-form: Kuwata, J. Am. Chem. Soc. 59, 2509 (1937); Harispe et al., Bull. Soc. Chim. Fr. 1964, 1035; of dl-form: Kuwata, loc. cit. Stereochemistry: Carlson et al., Tetrahedron Lett. 1968, 5941.
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