
CAS Name: N-[4-[(4-Aminophenyl)sulfonyl]phenyl]glycine
Additional Names: N-p-sulfanilylphenylglycine; p-amino-p'-(carboxymethylamino)diphenyl sulfone; 4-carboxymethylamino-4'-aminodiphenylsulfo...
Literature References: Prepn: Jackson, J. Am. Chem. Soc. 70, 680 (1948); CH 254803 and CH 278482 (1949, 1952, to Cilag Ltd.); Rawlins, US 2589211 (1952 to Parke, Davis).
CAS Name: 1H-Indole-3-butanoic acid
Additional Names: indole-3-butyric acid; 4-(3-indolyl)butyric acid
Trademarks: Seradix (Rhone-Poulenc)
Percent Composition: C 70.92%, H 6.45%, N 6.89%,...
Literature References: Prepn: Jackson, Manske, J. Am. Chem. Soc. 52, 5029 (1930); by heating indole, g-butyrolactone, and sodium hydroxide, followed by acidification of the product: Fritz, US 3051723 (1962 to Union Carbide); by decarboxylation of 2-carboxyindole-3-butyric acid: Bowman, Islip, Chem. Ind. (London) 1971, 154. Toxicity studies: Anderson et al., Proc. Soc. Exp. Biol. Med. 34, 138 (1936); Pesonen, Acta Endocrinol. 5, 409 (1950). Hypoglycemic effect in rats: Mirsky et al., Endocrinology 59, 715 (1956).
CAS Name: a-Phenyl-2-piperidinemethanol acetate
Additional Names: threo-1-acetoxy-1-phenyl-1-(2-piperidyl)methane; acetic acid a-phenyl-2-piperidylmethyl ester; 1-phenyl-1-(2'-piperidyl)-1-acet...
Literature References: Prepn: Jacob, Joseph, US 2928835 (1960 to Rhône-Poulenc).
CAS Name: 10,11-Dihydro-N,N,b-trimethyl-5H-dibenz[b,f]azepine-5-propanamine
Additional Names: 5-[3-(dimethylamino)-2-methylpropyl]-10,11-dihydro-5H-dibenz[b,f]azepine; 5-(3-dimethylamino-2-meth...
Literature References: Prepn: Jacob, Messer, Compt. Rend. 252, 2117 (1961). Toxicity studies: Okamoto, C.A. 72, 77299y (1970). Chemistry: Bever, Bredenstein, Dtsch. Apoth. Ztg. 113, 1562 (1973). Comprehensive description of the maleate: A. A. Al-Badr, Anal. Profiles Drug Subs. 12, 683-712 (1983).
CAS Name: 1-[3-[2-(Methylsulfonyl)-10H-phenothiazin-10-yl]propyl]-4-piperidinecarboxamide
Additional Names: 1-[3-[2-(methylsulfonyl)phenothiazin-10-yl]propyl]isonipecotamide; 10-[3-(4-carbamoyl...
Literature References: Prepn: Jacob, Robert, DE 1092476 (to Rhône-Poulenc), C.A. 56, 8723h (1962). Toxicity study: E. I. Goldenthal, Toxicol. Appl. Pharmacol. 18, 185 (1971).
CAS Name: 2-Ethyl-N,N,b-trimethyl-10H-phenothiazine-10-propanamine
Additional Names: 10-[3-(dimethylamino)-2-methylpropyl]-2-ethylphenothiazine; 3-ethyl-10-(3-dimethylamino-2-methylpropyl)pheno...
Literature References: Prepn: Jacob, Robert, US 2837518 (1958 to Rhône-Poulenc). Activity studies in pigs: Lambrerth, Aust. Vet. J. 44, 333 (1968). Biotransformation studies: Robinson, J. Pharm. Pharmacol. 18, 19 (1966).
CAS Name: 10-[3-(Dimethylamino)-2-methylpropyl]-10H-phenothiazine-2-carbonitrile
Additional Names: 2-cyano-10-(3-dimethylamino-2-methylpropyl)phenothiazine; 10-(3-dimethylamino-2-methylpropyl)-...
Literature References: Prepn: Jacob, Robert, US 2877224 (1959 to Rhône-Poulenc). Synthesis: Craig et al., J. Org. Chem. 26, 1138 (1961). Biotransformation studies: Robinson, J. Pharm. Pharmacol. 18, 19 (1966). Chemistry: Kiger, Kiger, Ann. Pharm. Fr. 23, 489 (1965).
CAS Name: N,N,b-Trimethyl-10H-phenothiazine-10-propanamine 5,5-dioxide
Additional Names: 10-(3-dimethylamino-2-methylpropyl)phenothiazine 5,5-dioxide; 3-(9,9-dioxo-10-phenothiazinyl)-2-methyl-1...
Literature References: Prepn: Jacob, Robert, US 2972612 (1961 to Rhône-Poulenc).
CAS Name: 4-Nitrophenylarsonic acid
Additional Names: p-nitrobenzenearsonic acid
Percent Composition: C 29.17%, H 2.45%, As 30.33%, N 5.67%, O 32.38%
Literature References: Prepn: Jacobs et al., J. Am. Chem. Soc. 40, 1580 (1918); Doak, Freedman, US 2653160 (1953 to the U.S.A. as represented by the Administrator of the Federal Security Agency); Ruddy, Starkey, Org. Synth. coll. vol. III, 665 (1955).
CAS Name: Sulfobutanedioic acid 1,4-bis(2-ethylhexyl) ester sodium salt
Additional Names: sulfosuccinic acid 1,4-bis(2-ethylhexyl) ester S-sodium salt; bis(2-ethylhexyl)sodium sulfosuccinate; d...
Literature References: Prepn: Jaeger, US 2028091; US 2176423 (1936, 1939, both to Am. Cyanamid). Structure and wetting power: Caryl, Ind. Eng. Chem. 33, 731 (1941). Comprehensive description: S. Ahuja, J. Cohen, Anal. Profiles Drug Subs. 2, 199-219 (1973); 12, 713-720 (1983). For structure see Docusate calcium.
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