
CAS Name: 5,5-Diphenyl-2-[2-(1-piperidinyl)ethyl]-1,3-dioxolan-4-one hydrochloride
Additional Names: 2-(b-N-piperidylethyl)-4,4-diphenyl-1,3-dioxolan-5-one hydrochlorideTrademarks: Rowapraxin (...
Literature References: Prepn: M. Pailer et al., Monatsh. Chem. 99, 891 (1968); GB 1109959 and BE 719230 (1968, 1969 to Rowa-Wagner). Pharmacology and acute toxicity: K. Morsdorf, H. Wengenroth, Pharmacology 3, 193 (1970).
CAS Name: (6b,11b)-17,21-Bis(acetyloxy)-2-bromo-6,9-difluoro-11-hydroxypregna-1,4-diene-3,20-dione
Additional Names: 2-bromo-6b,9-difluoro-11b,17,21-trihydroxypregna-1,4-diene-3,20-dione 17,21-...
Literature References: Prepn: M. Riva, L. Toscano, DE 2508136; M. Riva et al., US 4226862 (1975, 1980 both to Pierrel); L. Toscano et al., J. Med. Chem. 20, 213 (1977). Physico-chemical and analytical studies: eidem, Arzneim.-Forsch. 27, 1636 (1977). Pharmacology: A. Bianchetti et al., ibid. 2096. Clinical study: B. Palmerio, P. Magnani, ibid. 2404. Toxicological study: L. Casilli et al., ibid. 2102.
CAS Name: Trifluoromethanesulfonic acid trimethylsilyl ester
Additional Names: trimethylsilyltrifluoromethane sulfonate
Percent Composition: C 21.62%, H 4.08%, F 25.64%, O 21.60%, S 14.43%, ...
Literature References: Prepn: M. Schmeisser et al., Ber. 103, 868 (1970); H. W. Roesky, H. H. Giere, Z. Naturforsch. 25B, 773 (1970); D. Haebich, F. Effenberger, Synthesis 1978, 755; T. Morita et al., ibid. 1981, 745. As catalytic reagent: H. Vorbrueggen, K. Krolikiewicz, Angew. Chem. Int. Ed. 14, 421 (1975); as silylating agent: G. A. Olah et al., J. Org. Chem. 46, 5212 (1981).
CAS Name: 3,6-Acridinediamine
Additional Names: 3,6-diaminoacridine; 2,8-diaminoacridine
Percent Composition: C 74.62%, H 5.30%, N 20.08%
Literature References: Prepn: M. Schöpff, Ber. 27, 2320 (1894); DE 230412 (1910 to Cassella), C.A. 5, 2734 (1911); W. P. Thompson, GB 137214 (1919 to Poulenc Frères), C.A. 14, 1445 (1920); A. Albert, J. Chem. Soc. 1941, 121, 484; 1947, 244. Toxicity study: S. D. Rubbo, Br. J. Exp. Pathol. 28, 1 (1947). Review: The Acridines, A. Albert, Ed. (St. Martin's Press, New York, 2nd ed., 1966) pp 300-302; Acridines, R. M. Acheson, Ed. (Interscience, New York, 1956) pp 341-344.
CAS Name: 5-[Bis(carboxymethyl)amino]-2-carboxy-4-cyano-3-thiopheneacetic acid
Additional Names: 2-[N,N-di(carboxymethyl)amino]-3-cyano-4-carboxymethylthiophene-5-carboxylic acid
Percent Com...
Literature References: Prepn: M. Wierzbicki et al., EP 415850; eidem, US 5128367 (1991, 1992 both to Adir Co.).
CAS Name: 4-Amino-N-[2-(diethylamino)ethyl]benzamide monohydrochloride
Additional Names: procaine amide hydrochloride
Trademarks: Amisalin (Daiichi); Novocamid (Hoechst); Procamide (Sintesa)...
Literature References: Prepn: M. Yamazaki et al., J. Pharm. Soc. Jpn. 73, 294 (1953); Y. Tashika, M. Kuranari, ibid. 1069. Comprehensive description: R. B. Poet, H. Kadin, Anal. Profiles Drug Subs. 4, 333-383 (1975).
CAS Name: 5-[[4-(Dimethylamino)phenyl]methylene]-2-thioxo-4-thiazolidinone
Additional Names: 5-[p-(dimethylamino)benzylidene]rhodanine
Percent Composition: C 54.52%, H 4.58%, N 10.60%, O 6.0...
Literature References: Prepn: Mackie, Misra, J. Chem. Soc. 1954, 3919.
CAS Name: N-[5-(1,1-Dimethylethyl)-1,3,4-thiadiazol-2-yl]benzenesulfonamide
Additional Names: N-(5-tert-butyl-1,3,4-thiadiazol-2-yl)benzenesulfonamide; 2-benzenesulfonamido-5-tert-butyl-1,3,4-t...
Literature References: Prepn: Macrae, Drain, GB 822947 (1959 to Smith Nephew), C.A. 54, 4622h (1960); FR M3389 (1965 to Rhône-Poulenc), C.A. 64, 3553a (1966). Pharmacodynamics: Bargeton et al., Arch. Int. Pharmacodyn. 153, 379 (1965).
CAS Name: 3,4,5-Trimethoxybenzoic acid 2-[4-[3-(2-chloro-10H-phenothiazin-10-yl)propyl]-1-piperazinyl]ethyl ester
Additional Names: 2-[4-[3-(2-chlorophenothiazin-10-yl)propyl]-1-piperazinyl]eth...
Literature References: Prepn: Magy. Kem. Lapja 17, 169 (1962), C.A. 57, 11314d (1962); Toldy et al., Acta Chim. Acad. Sci. Hung. 42, 351 (1964).
CAS Name: 2-(1,3,4-Oxadiazol-2-yl)phenol
Additional Names: 2-(o-hydroxyphenyl)-1,3,4-oxadiazole
Trademarks: Hypnazol (Logeais)
Percent Composition: C 59.26%, H 3.73%, N 17.28%, O 19.73%
Literature References: Prepn: Maillard et al., Bull. Soc. Chim. Fr. 1961, 529; Vincent et al., ibid. 1962, 1580; GB 902388 and Maillard et al., FR M379 C.A. 57, 15251g (1962) (both 1962 to Logeais Labs.).
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