
CAS Name: N-Cyclohexylcyclohexanamine
Additional Names: dodecahydrodiphenylamine
Percent Composition: C 79.49%, H 12.79%, N 7.72%
Literature References: Prepn by hydrogenation of equimolar amounts of cyclohexanone and cyclohexylamine: C. F. Winans, H. Adkins, J. Org. Chem. 54, 306 (1932); R. M. Robinson, W. C. Braaten, US 3154580 (1964 to Abbott). Forms crystalline derivatives with N-protected amino acids: E. Klieger et al., Ann. 640, 157 (1961). Review: T. S. Carswell, H. L. Morrill, Ind. Eng. Chem. 29, 1265 (1937).
CAS Name: (3b,5a)-Ergostan-3-ol
Percent Composition: C 83.51%, H 12.51%, O 3.97%
Literature References: Prepn by hydrogenation of ergosta-14,22-dien-7-one: Chen, Ber. 70, 1432 (1937).
CAS Name: 1-Ethyl-2-[3-(1-ethyl-2-methyl-4(1H)-quinolinylidene)-1-propenyl]-4-methylquinolinium iodide
Additional Names: 1-ethyl-2-[3-(1-ethyl-4(1H)-quinaldylidene)propenyl]lepidinium iodide; 1...
Literature References: Prepn by J. A. Aeschlimann as reported by Mills, Odams, J. Chem. Soc. 125, 1913 (1924). See also Beilstein 2nd suppl. vol. 23, p 284. Has photoconductive properties that increase sharply with a rise in temp and is classed as an O2-photoconductor: Meier, Z. Phys. Chem. (Leipzig) 208, 325 (1958). Gives a color reaction with magnesium ions: Babenko, Zh. Anal. Khim. 13, 496 (1958).
CAS Name: 3-Nitrobenzenamine
Additional Names: m-nitraniline
Percent Composition: C 52.18%, H 4.38%, N 20.28%, O 23.17%
Literature References: Prepn by nitration of aniline: Holleman et al., Ber. 44, 704 (1911); by reduction of m-dinitrobenzene: Brady et al., J. Chem. Soc. 1929, 2266; Kubota et al., J. Pharm. Soc. Jpn. 76, 801 (1956); Kuhn, US 2768209 (1956 to Ringwood); from m-nitrobenzoic acid: Snyder et al., J. Am. Chem. Soc. 75, 2014 (1953).
CAS Name: 4-Amino-N-(4,6-diethyl-1,3,5-triazin-2-yl)benzenesulfonamide
Additional Names: N1-(4,6-diethyl-s-triazin-2-yl)sulfanilamide; 2-sulfanilamido-4,6-diethyl-1,3,5-triazine; 4,6-diethyl-2-...
Literature References: Prepn by nucleophilic displacement of methoxy groups from 2-methoxy-4,6-disubstituted s-triazines with sulfanilamide anion: Taft et al., J. Med. Chem. 8, 784 (1965); Bader, US 3344137 (1967 to Am. Cyanamid). Pharmacological studies: Frisk, Hultman, Antimicrob. Agents Chemother. 1965, 672; Kruger-Thiemer et al., Chemotherapia 10, 325 (1966).
CAS Name: D-Gluconic acid d-lactone
Additional Names: glucono delta lactone; delta gluconolactone
Trademarks: Fujiglucon (Fujisawa)
Percent Composition: C 40.45%, H 5.66%, O 53.89%
Literature References: Prepn by oxidation of glucose with bromine water: Isbell, Pigman, J. Res. Natl. Bur. Stand. 10, 337 (1933); by oxidation of glucose in Acetobacter suboxydans: King, Cheldelin, Biochem. J. 68, 31P (1958). Structure: J. Stanék et al., The Monosaccharides (Academic Press, New York, 1963) p 271.
CAS Name: 1-[2-(3-Methylbutoxy)-2-phenylethyl]pyrrolidine
Additional Names: 1-[b-(isopentyloxy)phenethyl]pyrrolidine; N-(2-phenyl-2-isoamyloxy)ethylpyrrolidine
Percent Composition: C 78.11%,...
Literature References: Prepn by reacting styrene and isoamyl alcohol with t-butyl hypobromite and then condensing the product with pyrrolidine: Mauvernay, Busch, DE 1811767 (1969 to C.E.R.M.), C.A. 72, 21607e (1970). Identification of urinary metabolites in humans and dogs: M. Constantin et al., Arzneim.-Forsch. 26, 80 (1976). Pharmcokinetics: M. Constantin, J. F. Pognat, ibid. 28, 646 (1978).
CAS Name: Dimethylphosphoric acid 3,5,6-trichloro-2-pyridinyl ester
Additional Names: O,O-dimethyl-O-3,5,6-trichloro-2-pyridyl phosphateTrademarks: Torelle (Dow)
Percent Composition: C 27.43...
Literature References: Prepn by reaction of 3,5,6-trihalo-2-pyridinol with phosphoryl chloride: Rigterink, Kenaga, J. Agric. Food Chem. 14, 304 (1966).
CAS Name: 2,3,5,6-Tetramethyl-2,5-cyclohexadiene-1,4-dione
Additional Names: tetramethyl-p-benzoquinone
Percent Composition: C 73.15%, H 7.37%, O 19.49%
Literature References: Prepn by reduction of dinitrodurene: Smith, Org. Synth. vol. 10, 40 (1930); Smith, Dobrovolny, J. Am. Chem. Soc. 48, 1420 (1926); by condensation of 2,3-diketopentane with itself in presence of alkalies: von Pechmann, Ber. 21, 1420 (1888); by the action of alkalies on 3,3-dichloropentan-2-one: Faworsky, J. Prakt. Chem. [2] 51, 538 (1895).
CAS Name: 5-Amino-2-hydroxybenzoic acid
Additional Names: 5-aminosalicylic acid; 5-amino-2-hydroxybenzene-1-carboxylic acid; m-aminosalicylic acid; fisalamine; mesalazine; 5-ASA
Trademarks: ...
Literature References: Prepn by reduction of m-nitrobenzoic acid with Zn dust and HCl: H. Weil et al., Ber. 55B, 2664 (1922); by electrolytic reduction: Le Guyader, Peltier, Compt. Rend. 253, 2544 (1961). Use in manufacture of dyes: GB 751386 (1956 to J. R. Geigy). Identification as active metabolite of sulfasalazine, q.v.: A. K. Azad Khan et al., Lancet 2, 892 (1977); P. A. M. Van Hees et al., Gut 21, 632 (1980). HPLC determn in serum: E. Brendel et al., J. Chromatogr. 385, 299 (1987). Bioavailability, plasma level and excretion: S. N. Rasmussen et al., Gastroenterology 83, 1062 (1982). Clinical evaluation in Crohn's disease: eidem, ibid. 85, 1350 (1983). Clinical trials in ulcerative colitis: M. Campieri et al., Lancet 2, 270 (1981); L. S. Friedman et al., Am. J. Gastroenterol. 81, 412 (1986); in comparison with olsalazine, q.v.: S. S. Rao et al., Scand. J. Gastroenterol. 22, 332 (1987). Brief review: G. Friedman, Am. J. Gastroenterol. 81, 141-144 (1986). Review of clinical efficacy in colonic diverticulosis: A. Tursi, Expert Opin. Pharmacother. 6, 69-74 (2005).
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