
CAS Name: 1,3-Naphthalenediol
Additional Names: 1,3-dihydroxynaphthalene
Percent Composition: C 74.99%, H 5.03%, O 19.98%
Literature References: Prepn by cyclization of ethyl phenylacetoacetate: Soliman, West, J. Chem. Soc. 1944, 53; by heating 1-amino-3-hydroxy-4-naphthalenesulfonic acid in acidic soln: Meyer, Bloch, Org. Synth. 25, 73 (1945); from 1,3-naphtholsulfonic acid: Kozlov, Odintsov, J. Appl. Chem. (USSR) 17, 219 (1944); Kozlov et al., Zh. Prikl. Khim. 35, 880 (1962).
CAS Name: 2-Phenylbicyclo[2.2.0]hexa-2,5-diene
Percent Composition: C 93.46%, H 6.54%
Literature References: Prepn by decompn of cyclobutadieneiron tricarbonyl with ceric ammonium nitrate in the presence of phenylacetylene: Burt, Pettit, Chem. Commun. 1965, 517.
CAS Name: 4-Sulfobenzenediazonium inner salt
Additional Names: DABS; diazotized sulfanilic acid ; Pauly's reagent; sulfanilic acid diazonium salt
Percent Composition: C 39.13%, H 2.19%, N 15...
Literature References: Prepn by diazotization of sulfanilic acid: E. Fischer, Ann. 190, 67 (1878); K. B. Whetsel et al., J. Am. Chem. Soc. 78, 3360 (1956); G. Kaupp et al., Chem. Eur. J. 8, 1395 (2002). Crystal structure.: C. Bugg et al., Acta Crystallogr. 17, 767 (1964). Use as denaturant for membrane proteins: R. T. Giaquinta et al., Arch. Biochem. Biophys. 162, 200 (1974); M.-J. Bouchet et al., J. Med. Chem. 30, 2222 (1987); of protein components: S. K. Nishimoto et al., Anal. Biochem. 216, 156 (1994). Determn of bilirubin: J. B. Landis, H. L. Pardue, Clin. Chem. 24, 1690 (1978); P. Fossati et al., ibid. 35, 173 (1989); of phenols: C. Baiocchi et al., Anal. Lett. 15, 1539 (1982); M. C. Quintero et al., Talanta 36, 717 (1989); of halides: M. Pandey et al., Analyst 123, 2319 (1998); S. Gosain et al., J. AOAC Int. 82, 167 (1999).
CAS Name: 1,1',3,3'-Tetrahydro-3,3'-dihydroxy-[3,3'-bi-2H-indole]-2,2'-dione
Additional Names: 3,3'-dihydroxy-[3,3'-biindoline]-2,2'-dione; 3,3'-dihydroxy-3,3'-dihydroisoindigo; isatyde
Perc...
Literature References: Prepn by dimerization reduction of isatin with ammonium hydrosulfide: Laurent, Ann. Chim. 3, 372 (1841); by piperidine-catalyzed condensation of isatin and dioxindole: Heller, Ber. 37, 943 (1904); Wahl, Hansen, Compt. Rend. 178, 393 (1924); from isatin and acenaphthene in sunlight: Oliveri-Mandala, Deleo, Gazz. Chim. Ital. 79, 337 (1949). Structure: Lefèvre, Bull. Soc. Chim. Fr. 19, 113 (1916); Sumpter, J. Am. Chem. Soc. 54, 2917 (1932); Bergmann, ibid. 77, 1549 (1955).
CAS Name: Ethanethioic acid
Additional Names: thiolacetic acid; thiacetic acid
Percent Composition: C 31.56%, H 5.30%, O 21.02%, S 42.12%
Literature References: Prepn by distilling glacial acetic acid with phosphorus pentasulfide: Kekulé, Ann. 90, 309 (1854); from acetic anhydride and hydrogen sulfide: Ellingboe, Org. Synth. 31, 105 (1951).
CAS Name: [4R-(4a,4ab,5ab,6a,12ab)]-4-(Dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,6,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-2-naphthacenecarboxamide
Additional Names: epitetracycline
CAS Name: 2-Chloro-1-(difluoromethoxy)-1,1,2-trifluoroethane
Additional Names: 2-chloro-1,1,2-trifluoroethyl difluoromethyl ether; methylfluretherTrademarks: Alyrane (Baxter); Efrane (Abbott); ...
Literature References: Prepn by fluorination of the corresp dichloromethyl ether: R. C. Terrell, GB 1138406; idem, US 3469011; US 3527813 (1969, 1969, 1970 all to Air Reduction). Synthesis and anesthetic properties: R. C. Terrell et al., J. Med. Chem. 14, 517 (1971); 15, 604 (1972). Enantiomeric resolution: J. Meinwald et al., Science 251, 560 (1991).
Additional Names: Phosphorus sesquisulfide; trisulfurated phosphorus
Percent Composition: P 56.29%, S 43.71%
Literature References: Prepn by fusing red phosphorus with sulfur: Stock, Ber. 43, 150 (1910); also from white phosphorus and sulfur in a high-boiling solvent such as a-chloronaphthalene: Frary, DE 309618 (1918); Chem. Zentralbl. 1919, II, 55.
CAS Name: 1,8-Dihydroxy-2,4,5,7-tetranitro-9,10-anthracenedione
Additional Names: 1,8-dihydroxy-2,4,5,7-tetranitroanthraquinone; 2,4,5,7-tetranitrochrysazin; chrysammic acid
Percent Composit...
Literature References: Prepn by heating chrysazin with fuming nitric acid: Liebermann, Ann. 183, 193 (1876). Structure: Robinson, Simonsen, J. Chem. Soc. 95, 1088 (1909).
CAS Name: N,N-Dimethyl-1-naphthalenamine
Additional Names: 1-dimethylaminonaphthalene
Percent Composition: C 84.17%, H 7.65%, N 8.18%
Literature References: Prepn by heating in a closed tube 1-naphthylamine and methyl iodide in methyl alcohol: Landshoff, Ber. 11, 643 (1878); by heating 1-naphthylamine with dimethyl sulfate in sodium hydroxide in presence of pyridine: Germuth, J. Am. Chem. Soc. 51, 1556 (1929). Use: F. G. Germuth, Ind. Eng. Chem. Anal. Ed. 1, 28 (1929).
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