
CAS Name: 1,1-Cyclopentanedimethanol bis(phenylcarbamate)
Additional Names: 1,1-cyclopentanedimethanol dicarbanilate; cyclopentane-1,1-dimethanol bis(phenylcarbamate); 1,1-dihydroxymethylcyclop...
Literature References: Prepn: Bourdais, Bull. Soc. Chim. Fr. 1962, 266; E. Rosenberg, GB 904410 corresp to US 3067240 (both 1962 to Lab. Cassenne).
CAS Name: 2-(Ethylthio)-10-[3-(4-methyl-1-piperazinyl)propyl]phenothiazine
Additional Names: 3-ethylmercapto-10-(1'-methylpiperazinyl-4'-propyl)phenothiazine
Percent Composition: C 66.12%, H...
Literature References: Prepn: Bourquin et al., Helv. Chim. Acta 41, 1072 (1958).
CAS Name: N-[(4-Methoxyphenyl)methyl]-N',N'-dimethyl-N-2-pyridinyl-1,2-ethanediamine
Additional Names: 2-[(2-dimethylaminoethyl)(p-methoxybenzyl)amino]pyridine; N-p-methoxybenzyl-N',N'-dimethyl...
Literature References: Prepn: Bovet et al., C.R. Seances Soc. Biol. Ses Fil. 138, 99 (1944); Huttrer et al., J. Am. Chem. Soc. 68, 1999 (1946); Viaud, Prod. Pharm. 2, 53 (1947); Horclois, US 2502151 (1950 to Rhône-Poulenc). Toxicity: A. von Schlichtergroll, Arzneim.-Forsch. 7, 237 (1957); of the maleate: F. Hunziker et al., ibid. 13, 324 (1963).
CAS Name: N-[4-(1,1-Dimethylethoxy)phenyl]acetamide
Additional Names: 4'-tert-butoxyacetanilide
Trademarks: Tromal (Burroughs Wellcome)
Percent Composition: C 69.54%, H 8.27%, N 6.76%, O ...
Literature References: Prepn: Bowden, Green, J. Chem. Soc. 1954, 1795.
CAS Name: 5-Chloro-8-quinolinol
Additional Names: 5-chloro-8-hydroxyquinoline; 5-chloro-8-oxychinolin; cloxiquine
Trademarks: Chlorisept (Chinosolfabrik)
Percent Composition: C 60.19%, H ...
Literature References: Prepn: Bratz, Niementowski, Ber. 52, 189 (1919); Weizmann, Bograchov, J. Am. Chem. Soc. 69, 1222 (1947); Manske et al., Can. J. Res. 27F, 359 (1949). Crystal structure: T. Banerjee, N. N. Saha, Acta Crystallogr. C42, 1408 (1986).
CAS Name: 4-Amino-N-(2,6-dimethoxy-4-pyrimidinyl)benzenesulfonamide
Additional Names: N1-(2,6-dimethoxy-4-pyrimidinyl)sulfanilamide; 2,6-dimethoxy-4-sulfanilamidopyrimidine; 2,4-dimethoxy-6-sul...
Literature References: Prepn: Bretschneider, Klötzer, US 2703800 (1955 to Oesterr. Stickstoffwerke); eidem, Monatsh. Chem. 87, 136 (1956); Langley, GB 866843 (1961 to I.C.I.); Bretschneider et al., Monatsh. Chem. 92, 128 (1961); US 3127398 (1964 to Hoffmann-La Roche); Shepherd et al., J. Org. Chem. 26, 2764 (1961). Toxicity data: Seki et al., Arzneim.-Forsch. 15, 1441 (1965). Toxicological, chemotherapeutic and pharmacokinetic studies: Böhni et al., Chemotherapy 14, 195-226 (1969); see also Aviado et al., ibid. 37.
CAS Name: 2-Hydroxybenzoic acid 4-(acetylamino)phenyl ester
Additional Names: p-acetamidophenyl salicylate; acetylaminophenyl salicylate; acetyl-p-aminosalol; p-acetylaminophenol salicylic acid...
Literature References: Prepn: Brewster, J. Am. Chem. Soc. 40, 1136 (1918).
CAS Name: 4-Aminobenzoic acid butyl ester
Additional Names: butyl aminobenzoate; n-butyl p-aminobenzoate
Trademarks: Butesin (Abbott); Butoform; Planoform; Scuroforme
Percent Composition:...
Literature References: Prepn: Brill, J. Am. Chem. Soc. 43, 1322 (1921); Adams, Volwiler, US 1440652 (1923 to Abbott); GB 252870; C.A. 17, 1243 (1923); C.A. 21, 2478 (1927).
CAS Name: N-Acetylglycine compd with 4,4'-(1-triazene-1,3-diyl)bis(benzenecarboximidamide) (2:1)
Additional Names: N-acetylglycine compd with 4,4'-(diazoamino)dibenzamidine; diminazene diacetur...
Literature References: Prepn: Brodersen et al., US 2838485 (1958 to Hoechst); Stavrovskaya, Drusvyatskaya, C.A. 59, 15199a (1963). Mode of action: Festy et al., C.R. Seances Acad. Sci. Ser. D 271, 730 (1970). Chemotherapeutic characteristics: Schmulevich et al., Veterinariya (Moscow) 38, 23 (1961), C.A. 56, 13512b (1962). Review: Newton in Antibiotics vol. 3, J. W. Corcoran, F. E. Hahn, Eds. (Springer-Verlag, New York, 1975) pp 34-47.
CAS Name: (3a,5a)-21-(Acetyloxy)-3-hydroxypregnane-11,20-dione
Additional Names: 3a,21-dihydroxy-5a-pregnane-11,20-dione 21-acetate; 21-acetoxy-3a-hydroxy-5a-pregnane-11,20-dione; alphadolone a...
Literature References: Prepn: Brown, Kirk, J. Chem. Soc. C 1969, 1653; Davis et al., DE 2030402 and ZA 7003861 (both 1971 to Glaxo), C.A. 75, 20793n, 64114w (1971).
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