
CAS Name: [3b,4a,6a,7a,15a(R),16b]-4,9-Epoxycevane-3,4,6,7,14,15,16,20-octol 6,7-diacetate 15-(2-methylbutanoate)
Additional Names: protoverine 6,7-diacetate 15-(2-methylbutyrate); protoverine ...
Literature References: Prepd from protoveratrine B: Kupchan, Ayres, J. Am. Chem. Soc. 82, 2252 (1960); Kupchan, US 3009917 and US 3066144 (1962 to Wisconsin Alumni Res. Found.). Structure: Kupchan, Ayres, loc. cit.
CAS Name: 2-Pyridinamine
Additional Names: 2-aminopyridine
Percent Composition: C 63.81%, H 6.43%, N 29.77%
Literature References: Prepd from pyridine and sodamide: Tschitschibabin, Chem. Zentralbl. 1915, I, 1065; Wibaut, Rec. Trav. Chim. 42, 240 (1923); A. I. Vogel, Practical Organic Chemistry (Longmans, London, 3rd ed., 1959) p 1007; Gattermann-Wieland, Praxis des Organischen Chemikers (de Gruyter, Berlin, 40th ed., 1961) p 316.
CAS Name: 3-Aminobutanoic acid
Additional Names: b-amino-n-butyric acid
Percent Composition: C 46.59%, H 8.80%, N 13.58%, O 31.03%
Literature References: Prepd from pyrotartaric acid diamide: Weidel, Roithmer, Monatsh. Chem. 17, 185 (1896); from b-chlorobutyric acid ethyl ester and alcoholic NH3: Balbiano, Ber. 13, 312 (1880); from crotonic acid and concd NH3: Engel, Bull. Soc. Chim. [2] 50, 102 (1888); Curtius, Gumlich, J. Prakt. Chem. [2] 70, 204 (1904); Stadnikow, Chem. Zentralbl. 1909, II, 1988; see Fischer, Roeder, Ber. 34, 3755 (1901) footnote; Stoermer, Robert, Ber. 55, 1038 (1922). Prepn of HCl salt from b-aminobutyronitrile: Bruylants, Bull. Soc. Chim. Belg. 32, 259 (1923); Chem. Zentralbl. 1924, I, 1668. By reducing acetoacetic ester phenylhydrazone and saponifying the resulting ester: Fischer, Groh, Ann. 383, 338 (1911). The D(-)-form has been obtained by hydrolysis of its ester: Fischer, Scheibler, ibid. 346.
CAS Name: 2-Hydroxybenzoic acid copper salt
Percent Composition: C 49.78%, H 2.98%, Cu 18.81%, O 28.42%
Literature References: Prepd from reaction of CuSO4 with Na salicylate: Hanic, Michalov, Acta Crystallogr. 13, 299 (1960); Inoue et al., Inorg. Chem. 3, 239 (1964).
Additional Names: Pearson's creolin
Literature References: Prepd from refined coal-tar oils. Approx composition: Tar acids and oils 75- 77%; emulsifying soaps 15-17%; water 8-10%.
CAS Name: 6-Hydroxy-1,3-benzoxathiol-2-one
Additional Names: 6-hydroxy-2-oxo-1,3-benzoxathiole; thioxolone
Trademarks: Camyna (Nycomed); Stepin (Basotherm)
Percent Composition: C 49.99%, ...
Literature References: Prepd from resorcinol and ammonium thiocyanate in presence of copper sulfate: Werner, US 2332418 (1943 to Winthrop); Urushibara, Koga, Bull. Chem. Soc. Jpn. 29, 419 (1956); Berg, Fiedler, US 2886488 (1959 to Thomae). Formerly believed to be the 4-hydroxy isomer: Fiedler, Ber. 95, 1771 (1962).
CAS Name: 7-Hydroxy-4-methyl-2H-1-benzopyran-2-one
Additional Names: 7-hydroxy-4-methylcoumarin; 7-hydroxy-4-methyl-2-oxo-3-chromene; 4-methylumbelliferone; b-methylumbelliferone; imecromone; 4...
Literature References: Prepd from resorcinol and ethyl acetoacetate: Pechmann, Duisberg, Ber. 16, 2119 (1883); Russell, Frye, Org. Synth. 21, 23 (1941); Woods, Sapp, J. Org. Chem. 27, 3703 (1962). Use in determn of nitric acid: F. J. Welcher, Organic Analytical Reagents vol. 1 (Van Nostrand, New York, 1947) pp 214-215.
CAS Name: 2-Hydroxybenzoic acid monoammonium salt
Additional Names: salicylic acid monoammonium salt
Trademarks: Salicyl-Vasogen
Percent Composition: C 54.19%, H 5.85%, N 9.03%, O 30.94%
Literature References: Prepd from salicylic acid and aq NH3: Cahours, Ann. 52, 336 (1844).
CAS Name: Acetic acid 1-methylpropyl ester
Additional Names: acetic acid sec-butyl ester
Percent Composition: C 62.04%, H 10.41%, O 27.55%
Literature References: Prepd from sec-butanol and acetic anhydride: Altschul, J. Am. Chem. Soc. 68, 2605 (1946). Prepn of d-form: Kenyon et al., J. Chem. Soc. 1935, 1072; Bird, Tetrahedron 18, 1 (1962). Prepn of l- form: Kenyon et al., loc. cit. Manuf: Faith, Keyes Clark's Industrial Chemicals, F. A. Lowenheim, M. K. Moran, Eds. (Wiley-Interscience, New York, 4th ed., 1975) pp 171-177.
CAS Name: Seleninyl fluoride
Additional Names: selenyl fluoride
Percent Composition: F 28.58%, O 12.03%, Se 59.39%
Literature References: Prepd from selenium dioxide and fluorine: Aynsley et al., J. Chem. Soc. 1952, 1231; from selenium oxychloride and sodium fluoride: Tullock, Coffman, J. Org. Chem. 25, 2016 (1960); from selenium tetrafluoride and tellurium oxide: J. Carre et al., J. Fluorine Chem. 14, 139 (1979).
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