
CAS Name: N-9H-Fluoren-2-ylacetamide
Additional Names: 2-acetylaminofluorene; AAF; 2-FAA
Percent Composition: C 80.69%, H 5.87%, N 6.27%, O 7.17%
Literature References: Synthesis: Hayashi, Nakayama, J. Soc. Chem. Ind. Jpn. [Suppl] 36, 127B (1933). Carcinogenicity studies: R. H. Wilson et al., Cancer Res. 1, 595 (1941). Toxicity studies: Haley et al., Proc. Soc. Exp. Biol. Med. 143, 1117 (1973); 146, 648 (1974).
CAS Name: 3-(Acetylamino)-2,4,6-triiodo-5-[(methylamino)carbonyl]benzoic acid
Additional Names: 5-acetamido-2,4,6-triiodo-N-methylisophthalamic acid
Percent Composition: C 21.52%, H 1.48%, I...
Literature References: Synthesis: Hoey et al., J. Med. Chem. 6, 24 (1963).
CAS Name: 3,4-Dihydro-6-(trifluoromethyl)-2H-1,2,4-benzothiadiazine-7-sulfonamide 1,1-dioxide
Additional Names: 6-trifluoromethyl-3,4-dihydro-7-sulfamoyl-2H-1,2,4-benzothiadiazine 1,1-dioxide; ...
Literature References: Synthesis: Holdrege et al., J. Am. Chem. Soc. 81, 4807 (1959); Close et al., ibid. 82, 1132 (1960); Yale et al., ibid. 2042; Novello et al., J. Org. Chem. 25, 970 (1960). Numerous patents, e.g., Lund et al., US 3254076 (1966 to Lövens Kemiske Fabrik). Pharmacology: J. J. Piala et al., J. Pharmacol. Exp. Ther. 134, 273 (1961). Comprehensive description: C. E. Orzech et al., Anal. Profiles Drug Subs. 7, 297-317 (1978).
CAS Name: 6-(Trifluoromethyl)-2H-1,2,4-benzothiadiazine-7-sulfonamide 1,1-dioxide
Additional Names: 6-trifluoromethyl-7-sulfamoyl-4H-1,2,4-benzothiadiazine 1,1-dioxide; 6-trifluoromethyl-7-sulf...
Literature References: Synthesis: Holdrege et al., J. Am. Chem. Soc. 81, 4807 (1959); Yale et al., ibid. 82, 2042 (1960); US 3040042 (1962 to Olin Mathieson); GB 861809 (1961 to SKF).
CAS Name: N,N-Dimethyl-3-[1-(2-pyridinyl)ethyl]-1H-indene-2-ethanamine
Additional Names: 2-[1-[2-[2-(dimethylamino)ethyl]inden-3-yl]ethyl]pyridine; 3-[a-(2'-pyridyl)ethyl]-2-(b-dimethylaminoeth...
Literature References: Synthesis: Huebner et al., J. Am. Chem. Soc. 82, 2077 (1960); Huebner, US 2970149 (1961 to Ciba). Pharmacology: W. E. Barrett et al., Toxicol. Appl. Pharmacol. 3, 534 (1961).
CAS Name: N-[(4-Amino-2-methyl-5-pyrimidinyl)methyl]-N-[4-hydroxy-1-methyl-2-(propyldithio)-1-butenyl]formamide
Additional Names: 2-(2-methyl-4-aminopyrimidin-5-yl)methylformamido-5-hydroxy-2-p...
Literature References: Synthesis: Matsukawa, Kawasuki, J. Pharm. Soc. Jpn. 73, 216 (1953), C.A. 48, 2071 (1954); Matsukawa et al., J. Vitaminol. 1, 13 (1954); Fujiwara et al., US 2833768 (1958 to Takeda), cf. FR 1068459 (1954 to Takeda). Structural studies: Nishikawa et al., Chem. Pharm. Bull. 17, 932 (1969). Metabolism: Suzuoki-Ziro et al., J. Biochem. 58, 279 (1965); Nishikawa et al., J. Pharmacol. Exp. Ther. 157, 589 (1967).
CAS Name: 4-Butoxy-N-hydroxybenzeneacetamide
Additional Names: 2-(p-butoxyphenyl)acetohydroxamic acid; 2-[p-(butyloxy)phenyl]acetohydroxamic acidTrademarks: Droxarol (Pharmos); Droxaryl (Contin...
Literature References: Synthesis: N. P. Buu-Hoï et al., Compt. Rend. 261, 2259 (1965); eidem, BE 661226; eidem, US 3479396 (1965, 1969 to Madan). Pharmacology and toxicology: Lambelin et al., Med. Pharmacol. Exp. 15, 545 (1966).
CAS Name: 4-Amino-N-(1-phenyl-1H-pyrazol-5-yl)benzenesulfonamide
Additional Names: N'-(1-phenylpyrazol-5-yl)sulfanilamide; 1-phenyl-5-sulfanilamidopyrazole; 3-(p-aminobenzenesulfonamido)-2-phen...
Literature References: Synthesis: Schmidt, Druey, Helv. Chim. Acta 41, 309 (1958); Druey, Schmidt, US 2858309 (1958 to Ciba). Toxicity study: Seki et al., Arzneim.-Forsch. 15, 1441 (1965).
CAS Name: a-D-Glucopyranose 1-(3,4,5-trihydroxybenzoate)
Additional Names: a-D-glucopyranose-1-gallate; 1-galloyl-a-D-glucose
Percent Composition: C 46.99%, H 4.85%, O 48.15%
Literature References: Synthesis: Schmidt, Herok, Ann. 587, 63 (1954); Schmidt, Schmadel, ibid. 649, 149 (1961).
CAS Name: 5-Hydroxynorvaline
Additional Names: a-amino-d-hydroxy-n-valeric acid; 2-amino-5-hydroxypentanoic acid
Percent Composition: C 45.10%, H 8.33%, N 10.52%, O 36.05%
Literature References: Synthesis: Sörensen, Bull. Soc. Chim. Fr. 33, 1052 (1904); Plieninger, Ber. 83, 271 (1950); Gaudry, Can. J. Chem. 29, 544 (1951). Enzymatic resolution: Berlinguet, Gaudry, J. Biol. Chem. 198, 765 (1952).
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