
CAS Name: 2-[[3-(Trifluoromethyl)phenyl]amino]benzoic acid
Additional Names: N-(a,a,a-trifluoro-m-tolyl)anthranilic acid; 3'-trifluoromethyldiphenylamine-2-carboxylic acidTrademarks: Achless (T...
Literature References: Prepn from m-aminobenzotrifluoride and o-iodobenzoic acid: Wilkinson, Finar, J. Chem. Soc. 1948, 32. Pharmacology: Winder et al., Arthritis Rheum. 6, 36 (1963); 12, 472 (1969). Antiviral activity: Inglot, J. Gen. Virol. 4, 203 (1969). Toxicity data: Zoni et al., Farmaco Ed. Sci. 26, 191 (1971). Comprehensive description: E. Abignente, P. deCaprariis, Anal. Profiles Drug Subs. 11, 313-346 (1982).
CAS Name: 5'-Inosinic acid
Additional Names: 5-inosinic acid; muscle inosinic acid; t-inosinic acid; hypoxanthine riboside-5-phosphoric acid; IMP
Percent Composition: C 34.49%, H 3.76%, N 16...
Literature References: Prepn from meat extract: Levene, Bass, Nucleic Acids (New York, 1931) p 229; from dried sardines: Yoshida, Kageyama, JP 56 732 (1956 to Ajinomoto), C.A. 51, 3870b (1957). Structure: Levene, Bass, op. cit., pp 187-192; Bredereck, Ber. 66, 198 (1933); Levene, Tipson, J. Biol. Chem. 111, 313 (1935). Also prepd from muscle by enzymatic deamination of muscle adenylic acid: Ostern, Biochem. Z. 254, 65 (1932); by hydrolysis of inosine triphosphate: Kleinzeller, Biochem. J. 36, 729 (1942). Studies on the enzymatic synthesis: Greenberg, J. Biol. Chem. 190, 611 (1951); Korn et al., ibid. 217, 875 (1955). Microbial fermentation method using mutant strains of Micrococcus glutamicus: Kinoshita et al., US 3232844 (1966 to Kyowa).
CAS Name: Methanedisulfonic acid
Percent Composition: C 6.82%, H 2.29%, O 54.49%, S 36.40%
Literature References: Prepn from methane + sulfur trioxide: Snyder, Grosse, US 2493038 (1950 to Houdry Process); by H2SO4 oxidation of acetic acid: Schwab, Neuwirth, Ber. 90, 567 (1957); from MeSO3H + SO3: Crowder, Gilbert, US 2842589 (1958 to Allied Chem.). Prepn of aluminum salt: Christian, Jenkins, J. Am. Pharm. Assoc. 39, 633 (1950); US 2504107 (1950 to Purdue Res. Found.).
CAS Name: Nitric acid methyl ester
Percent Composition: C 15.59%, H 3.93%, N 18.18%, O 62.30%
Literature References: Prepn from methanol and nitric acid in the presence of sulfuric acid: Black, Babers, Org. Synth. coll. vol. II, 412 (1943).
CAS Name: 1-[4-[[2-O-(6-Deoxy-a-L-mannopyranosyl)-b-D-glucopyranosyl]oxy]-2,6-dihydroxyphenyl]-3-(3-hydroxy-4-methoxyphenyl)-1-propanone
Additional Names: 3,5-dihydroxy-4-(3-hydroxy-4-methoxyhy...
Literature References: Prepn from naringen, a flavanone glycoside occurring naturally in grapefruit: Horowitz, Gentile, US 3087821 and US 3375242 (1963, 1968, both to U.S. Secy. Agr.); Robertson et al., Ind. Eng. Chem. Prod. Res. Dev. 13, 125 (1974). Sweetening effect: Inglett et al., J. Food Sci. 34, 101 (1969). Chromatography: Gentile, Horowitz, J. Chromatogr. 63, 467 (1971); J. F. Fisher, J. Agric. Food Chem. 25, 682 (1977). Subchronic oral toxicity study: B. A. R. Lina et al., Food Chem. Toxicol. 28, 507 (1990). Review: P. J. Pratter, Perfum. Flavor. 5, 12-18 (1981).
CAS Name: 2-Propenoic acid butyl ester
Additional Names: acrylic acid n-butyl ester
Percent Composition: C 65.60%, H 9.44%, O 24.97%
Literature References: Prepn from n-butanol and methyl acrylate: Rehberg, Org. Synth. coll. vol. III, 146 (1955). Toxicity study: H. F. Smyth et al., Arch. Ind. Hyg. Occup. Med. 4, 119 (1951).
Percent Composition: Ag 52.03%, Cl 17.10%, O 30.87%
Literature References: Prepn from NOClO4 + AgBr: Markowitz et al., J. Inorg. Nucl. Chem. 16, 159 (1960).
Additional Names: o-Nitraniline
Percent Composition: C 52.18%, H 4.38%, N 20.28%, O 23.17%
Literature References: Prepn from o-dinitrobenzene: Meisenheimer, Hesse, Ber. 52, 1166 (1919); from o-nitroaniline-p-sulfonic acid: Ehrenfeld, Puterbaugh, Org. Synth. coll. vol. I, 388 (1941); from y-o-dinitrosobenzene: Boyer et al., J. Am. Chem. Soc. 77, 5688 (1955).
CAS Name: 2-Aminobenzenesulfonic acid
Additional Names: o-sulfanilic acid; o-anilinesulfonic acid
Percent Composition: C 41.61%, H 4.07%, N 8.09%, O 27.71%, S 18.51%
Literature References: Prepn from o-nitrobenzenesulfonyl chloride: Wertheim, Org. Synth. coll. vol. II, 271 (1943).
Additional Names: Sodium 4-(hydroxymercuri)-2-nitrophenolate; sodium hydroxymercuri-o-nitrophenolate; 4-(hydroxymercuri)-2-nitrophenol sodium salt
Percent Composition: C 19.08%, H 1.07%, Hg 53....
Literature References: Prepn from o-nitrophenol and Hg(OCOCH3)2: Schamberg et al., US 1390972 (1922). Structure: Malcolm, J. Bacteriol. 22, 403 (1931).
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