
CAS Name: [3-Ethyl-4-oxo-5-(1-piperidinyl)-2-thiazolidinylidene]acetic acid ethyl ester
Additional Names: 3-ethyl-4-oxo-5-piperidino-D2,a-thiazolidineacetic acid ethyl esterTrademarks: Coleflux...
Literature References: Prepn: G. Satzinger, Ann. 665, 150 (1963); G. Satzinger et al., DE 2414345 (1975 to Goedecke), corresp to US 3971794 (1976 to Warner-Lambert). Metabolism and pharmacokinetics: K. O. Vollmer, F. W. Koss, Arch. Int. Pharmacodyn. Ther. 198, 312 (1972). Mechanism of action: F. W. Koss et al., ibid. 333. Series of articles on synthesis, pharmacology, toxicology and clinical studies: Arzneim.-Forsch. 27, 463-526 (1977). Toxicity data: M. Herrmann et al., ibid. 467.
CAS Name: 4-Nitro-1,1'-biphenyl
Additional Names: 4-nitrobiphenyl; p-nitrodiphenyl; PNB
Percent Composition: C 72.35%, H 4.55%, N 7.03%, O 16.06%
Literature References: Prepn: G. Schultz, Ann. 174, 210 (1874); O. Kühling, Ber. 28, 42 (1895); E. Bamberger, ibid. 404; R. L. Jenkins et al., Ind. Eng. Chem. 22 (1), 31 (1930); K. Dimroth et al., Ber. 101, 2215 (1968). Crystal structure: M. Prasad et al., J. Indian Chem. Soc. 13, 519 (1936), C.A. 31, 12715 (1937). Review of carcinogenic risk: IARC Monographs vol. 4, 113-117 (1974).
CAS Name: 1-(Ethylsulfonyl)-4-fluorobenzene
Additional Names: ethyl p-fluorophenyl sulfone; p-fluorophenyl ethyl sulfone
Trademarks: Bripadon; Caducid (Wassermann)
Percent Composition: C ...
Literature References: Prepn: G. Thuillier et al., Compt. Rend. 248, 2492 (1959); P. Rumpf, G. Thuillier, FR M399; eidem, US 3084101 (1962, 1963 both to Centre Nat. Recher. Scient.); A. A. Mignot, P. Rumpf, Bull. Soc. Chim. Fr. 1968, 435. Pharmacology: J. Thuillier et al., Proc. 3rd Meet Coll. Int. Neuro-Psychopharmacol. 1962, 317-326 (Publ. 1964). Clinical evaluation: H. Akimoto, S. Taen, ibid. 326. Gas chromatography: E. Marozzi et al., Farmaco Ed. Prat. 31, 180 (1976).
CAS Name: 1-Ethyl-1,4-dihydro-7-methyl-4-oxo-1,8-naphthyridine-3-carboxylic acid
Additional Names: 3-carboxy-1-ethyl-7-methyl-1,8-naphthyridin-4-one; 1-ethyl-7-methyl-1,8-naphthyridin-4-one-3-c...
Literature References: Prepn: G. Y. Lesher et al., J. Med. Pharm. Chem. 5, 1063 (1962); G. Y. Lesher, M. D. Gruett, BE 612258; eidem, US 3590036 (1962, 1971 both to Sterling Drug). Mechanism of action studies: G. J. Bourguignon et al., Antimicrob. Agents Chemother. 4, 479 (1973); W. A. Goss, T. M. Cook, Antibiotics vol. 3, J. W. Corcoran, F. E. Hahn, Eds. (Springer-Verlag, New York, 1975) pp 174-196; A. M. Pedrini, ibid. vol. 5 (pt. 1), F. E. Hahn, Ed. (1979) pp 154-175; H. T. Wright et al., Science 213, 455 (1981). Comprehensive description: P. E. Grubb, Anal. Profiles Drug Subs. 8, 371-397 (1979).
CAS Name: N-Acetyl-DL-leucine compd with 2-aminoethanol (1:1)
Additional Names: monoethanolamine DL-acetylleucinate; DL-acetylleucine monoethanolamine salt; monoethanolamine salt of a-acetamido...
Literature References: Prepn: Gailliot et al., US 2941924 (1960 to Rhône-Poulenc).
CAS Name: 2-(4-Chlorophenoxy)-2-methylpropanoic acid
Additional Names: 2-(p-chlorophenoxy)-2-methylpropionic acid; a-(p-chlorophenoxy)isobutyric acid; chlorophibrinic acid
Trademarks: Arteri...
Literature References: Prepn: Galimberti, Defranceschi, Gazz. Chim. Ital. 77, 431 (1947); Gilman, Wilder, J. Am. Chem. Soc. 77, 6644 (1955); Jones et al., GB 860303 (1961 to I.C.I.). Prepn and resolution of isomers: Witiak et al., J. Med. Chem. 11, 1086 (1968). Activity thought to be due to its displacement of thyroxin and its inhibition of cholesterol biosynthesis. See Chang et al., Biochem. Pharmacol. 16, 2053 (1967); Walsh et al., Arch. Biochem. Biophys. 130, 7 (1969); Witiak et al., J. Med. Chem. 14, 754 (1971). Metabolism: Almirante et al., Boll. Chim. Farm. 108, 292 (1969).
CAS Name: (1,3,5-Triazine-2,4,6-triyltrinitrilo)hexakismethanol
Additional Names: (s-triazine-2,4,6-triyltrinitrilo)hexamethanol; hexakis(hydroxymethyl)melamine
Trademarks: Resloom M 75 (Mon...
Literature References: Prepn: Gams et al., Helv. Chim. Acta 24, 302E (1941); Widmer, Fisch, US 2387547 (1945 to Ciba).
CAS Name: 6-[4-(Trifluoromethyl)phenyl]-3-morpholinone
Additional Names: 6-(a,a,a-trifluoro-p-tolyl)-3-morpholinonePercent Composition: C 53.88%, H 4.11%, F 23.24%, N 5.71%, O 13.05%
Literature References: Prepn: Gannon, Poos, US 3308121 (1967 to McNeil).
Additional Names: Lead sulfocyanate
Percent Composition: C 7.43%, N 8.66%, Pb 64.08%, S 19.83%
Literature References: Prepn: Gardner, Weinberger, Inorg. Synth. 1, 85 (1939).
CAS Name: Butanoic acid pentyl ester
Percent Composition: C 68.31%, H 11.47%, O 20.22%
Literature References: Prepn: Gartenmeister, Ann. 233, 269 (1886). Toxicity study: P. M. Jenner et al., Food Cosmet. Toxicol. 2, 327 (1964).
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