
Additional Names: Potassium acid fluoride; potassium hydrogen fluoride
Percent Composition: F 48.65%, H 1.29%, K 50.06%
Literature References: Prepd according to the eq KOH + 2HF = KHF2 + H2O: Lange, Eichler, Z. Phys. Chem. 129, 285 (1927); Kwasnik in Handbook of Preparative Inorganic Chemistry vol. 1, G. Brauer, Ed. (Academic Press, New York, 2nd ed., 1963) p 237. Made commercially from potassium carbonate and hydrofluoric acid.
CAS Name: (SP-4-1)-Hydrogen tetrachloroaurate(1-)
Additional Names: hydrochloroauric acid; aurochlorohydric acid; chloroauric acid
Percent Composition: Au 57.97%, Cl 41.74%, H 0.30%
Literature References: Prepd according to the equation 2Au + 3Cl2 + 2HCl ® 2HAuCl4: Thomsen, Ber. 16, 1585 (1883); Biltz, Wein, Z. Anorg. Allg. Chem. 148, 192 (1925).
CAS Name: Sodium tetrafluoroborate
Additional Names: sodium borofluoride
Percent Composition: B 9.85%, F 69.22%, Na 20.94%
Literature References: Prepd according to the equation 2H3BO3 + 8HF + Na2CO3 ® 2NaBF4 + 7H2O + CO2: Balz, Wilke-Dörfurt, Z. Anorg. Allg. Chem. 159, 197 (1927); Kwasnik in Handbook of Preparative Inorganic Chemistry vol. 1, G. Brauer, Ed. (Academic Press, New York, 2nd ed., 1963) p 222.
CAS Name: Dicarbonic acid diethyl ester
Additional Names: oxydiformic acid diethyl ester; diethyl pyrocarbonate; diethyl oxydiformate; DEPCTrademarks: Baycovin
Percent Composition: C 44.45%,...
Literature References: Prepd according to the equation R1OOCCl + NaOCOOR2 ® R1OOCOCOOR2 + NaCl: Kovalenko, Zh. Obshch. Khim. 22, 1546 (1952); Thoma, Rinke, Ann. 624, 30 (1959); alternate method: Degering et al., J. Am. Pharm. Assoc. Sci. Ed. 39, 626 (1950). Review: Handbook of Food Additives, T. A. Furia, Ed. (Chemical Rubber Co., Cleveland, 1968) pp 181-185.
Additional Names: Nitrosonium tetrafluoroborate; nitrosyl borofluoride; nitrosyl fluoborate
Percent Composition: B 9.26%, F 65.06%, N 11.99%, O 13.70%
Literature References: Prepd according to the equation: 2 HBF4 + N2O3 ®2 NOBF4 + H2O: Wilke-Dörfurt, Balz, Z. Anorg. Allg. Chem. 159, 219 (1927); Balz, Mailänder, ibid. 217, 162 (1934); H. S. Booth, D. R. Martin, Boron Trifluoride and Its Derivatives (New York, 1949) p 133 sqq. Review of tetrafluoroborates: Sharp, Adv. Fluorine Chem. 1, 68-128 (1960).
CAS Name: Phosphoryl bromide
Additional Names: phosphoryl tribromide
Percent Composition: Br 83.61%, O 5.58%, P 10.80%
Literature References: Prepd according to the equation: 3PBr5 + P2O5 ® 5POBr3: Hönigschmid, Hirschbold-Wittner, Z. Anorg. Allg. Chem. 243, 355 (1940); Johnson, Nunn, J. Am. Chem. Soc. 63, 141 (1941); Booth, Seegmiller, Inorg. Synth. 2, 151 (1946).
CAS Name: (Dimethyldithiocarbamato)copper compd with copper chloride
Additional Names: dimethyldithiocarbamic acid copper salt complex with copper chloride; cuprous dimethyldithiocarbamate cupr...
Literature References: Prepd as monocuprous chloride complex [(CH3)2NCSSCu.CuCl]: Couillard, Racine, US 3037041 (1962 to Roussel-UCLAF). Prepd as dicuprous chloride complex [(CH3)2NCSSCu.2CuCl]: GB 825901 (1959 to UCLAF).
Percent Composition: C 36.74%, H 6.17%, O 57.09%
Literature References: Prepd as the sodium salt by reduction of sodium glucuronate with sodium amalgam in alkaline medium: Fischer, Piloty, Ber. 24, 525 (1891); from D-gulonic acid g-lactone: Rehorst, Naumann, ibid. 77, 24 (1944).
CAS Name: N,N-Dimethyl-N'-phenyl-N'-(2-thienylmethyl)-1,2-ethanediamine
Additional Names: N,N-dimethyl-N'-phenyl-N'-(2-thenyl)ethylenediamineTrademarks: Diatrin base (Warner-Chilcott)
Percen...
Literature References: Prepd by a sodamide condensation of N,N-dimethyl-N¢-phenylethylenediamine with 2-thenyl chloride in dry toluene: Leonard, Solmssen, J. Am. Chem. Soc. 70, 2066 (1948). Pharmacology and toxicology: N. Ercoli et al., J. Pharmacol. Exp. Ther. 93, 210 (1948).
CAS Name: 4-(Phenylamino)benzenesulfonic acid
Additional Names: 4-diphenylaminesulfonic acid; p-anilinobenzenesulfonic acid
Percent Composition: C 57.82%, H 4.45%, N 5.62%, O 19.25%, S 12.86...
Literature References: Prepd by acetylation followed by sulfonation of diphenylamine: Merz, Weith, Ber. 6, 1512 (1873); Gnehm, Werdenberg, Z. Angew. Chem. 12, 1027 (1899); Sarver, Kolthoff, J. Am. Chem. Soc. 53, 1902 (1931).
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