
CAS Name: 3,3'-Bis[(diethylamino)methyl]-5,5'-di-2-propenyl-[1,1'-biphenyl]-4,4'-diol
Additional Names: 5,5'-diallyl-a,a'-bis(diethylamino)-m,m'-bitolyl-4,4'-diol; 6,6'-diallyl-a,a'-bis(diethyl...
Literature References: Prepd by treating 2,2¢-diallyl-p,p¢-biphenol with diethylamine and formaldehyde: Burckhalter et al., J. Am. Chem. Soc. 68, 1894 (1946); Rawlins et al., US 2459338 (1949 to Parke, Davis).
CAS Name: 4-Amino-N-2-quinoxalinylbenzenesulfonamide
Additional Names: N1-(2-quinoxalinyl)sulfanilamide; 2-sulfanilamidoquinoxaline; N1-(2-quinoxalyl)sulfanilamide; sulfabenzpyrazineTrademarks:...
Literature References: Prepd by treating 2-aminoquinoxaline with acetylsulfanilyl chloride in the presence of pyridine and hydrolyzing the resulting acetyl deriv: Weijlard et al., J. Am. Chem. Soc. 66, 1957 (1944); Weijlard, Tishler, US 2404199 (1946 to Merck Co.). Anticoccidial spectrum: G. F. Mathis et al., Poult. Sci. 63, 1149 (1984). Evaluation of antibacterial and anticoccidial efficacy of mixture with trimethoprim: G. White, R. B. Williams, Vet. Rec. 113, 608 (1983); D. W. T. Piercy et al., ibid. 114, 60 (1984). Drug residue study in poultry muscle and liver: M. Patthy, J. Chromatogr. 275, 115 (1983). HPLC determn in rabbit plasma and urine: J. G. Eppel, J. J. Thiessen, J. Pharm. Sci. 73, 1635 (1984).
CAS Name: 3-Amino-2,7-naphthalenedisulfonic acid
Additional Names: 2-naphthylamine-3,6-disulfonic acid
Percent Composition: C 39.60%, H 2.99%, N 4.62%, O 31.65%, S 21.14%
Literature References: Prepd by treating 2-hydroxy-3,6-naphthalenedisulfonic acid with ammonium sulfite and ammonium hydroxide: Petitcolas, Josué, Bull. Soc. Chim. Fr. 1952, 89.
CAS Name: 4-Chloro-3,5-dimethylphenol
Additional Names: p-chloro-m-xylenol; 4-chloro-3,5-xylenol; parachlorometaxylenol; 2-chloro-m-xylenol; 2-chloro-5-hydroxy-m-xylene; 2-chloro-5-hydroxy-1,3-...
Literature References: Prepd by treating 3,5-dimethylphenol with Cl2 or SO2Cl2: Lesser, Gad, Ber. 56, 974, 976 (1923); von Auwers et al., Chem. Zentralbl. 1924, II, 2267, C.A. 19, 2339 (1925); Gladden, Cocker, US 2350677 (1944).
CAS Name: 2,5-Pyridinedicarboxylic acid
Percent Composition: C 50.31%, H 3.02%, N 8.38%, O 38.29%
Literature References: Prepd by treating 5-ethyl-2-picoline (aldehyde-collidine) with suitable oxidizing agents such as HNO3, KMnO4, or H2SeO3: Meyer, Staffen, Monatsh. Chem. 34, 517 (1913); Jordan, Ind. Eng. Chem. 44, 332 (1952); Kato, Bull. Chem. Soc. Jpn. 34, 636 (1961); by oxidation of 5-acetyl-2-methylpyridine: Binns, Swan, J. Chem. Soc. 1962, 2831; from the lutidine fraction of coal tar lutidine: Lukes et al., Collect. Czech. Chem. Commun. 26, 3044 (1961).
CAS Name: 5-Nitro-2-furancarboxaldehyde oxime
Additional Names: anti-5-nitro-2-furaldoxime
Trademarks: Micofur (Norwich)
Percent Composition: C 38.47%, H 2.58%, N 17.95%, O 41.00%
Literature References: Prepd by treating 5-nitrofurfural with hydroxylamine in alcohol: Ikeda, C.A. 50, 10701 (1956). Claimed in Stillman et al., US 2319481 (1943 to Norwich Pharmacal).
Additional Names: Acetobromamide
Percent Composition: C 17.41%, H 2.92%, Br 57.92%, N 10.15%, O 11.60%
Literature References: Prepd by treating a cooled (0-5°) soln of acetamide dissolved in bromine with ice cold aq 50% KOH, allowing to stand for 2-3 hr at 0-5°, treating with NaCl, and extracting with chloroform: Oliveto, Gerold, Org. Synth. 31, 17 (1951).
Percent Composition: H 4.50%, N 15.65%, O 35.75%, Se 44.10%
Literature References: Prepd by treating a soln of selenic acid with ammonia: Retgers, Z. Phys. Chem. 8, 36 (1891); King, J. Phys. Chem. 41, 797 (1937). Crystal structure: Gatlow, Acta Crystallogr. 15, 419 (1962).
CAS Name: Carboxymethyl ether cellulose sodium salt
Additional Names: sodium carboxymethylcellulose; sodium cellulose glycolate
Trademarks: Cethylose (Ascher); CMC (Stuart); Cel-O-Brandt; Gl...
Literature References: Prepd by treating alkali cellulose with sodium chloroacetate: Faith, Keyes Clark's Industrial Chemicals, F. A. Lowenheim, M. K. Moran, Eds. (Wiley-Interscience, New York, 4th ed., 1975) pp 235-238. Review and bibliography: Ott, Cellulose and Cellulose Derivatives, New York, 1946 (2nd ed., 1955).
CAS Name: 1,3-Dihydro-1-methyl-2H-imidazole-2-thione
Additional Names: 1-methylimidazole-2-thiol; 1-methyl-2-mercaptoimidazole; mercazolyl; thiamazole
Trademarks: Basolan; Danantizol; Favist...
Literature References: Prepd by treating aminoacetaldehyde diethyl acetal with methyl isothiocyanate: Wohl, Marckwald, Ber. 22, 1354 (1889); from thiocyanic acid and N-substituted amino acetals: Jones et al., J. Am. Chem. Soc. 71, 4000 (1949). Metabolism: D. S. Sitar, D. P. Thornhill, J. Pharmacol. Exp. Ther. 184, 432 (1973). Comprehensive description: H. Y. Aboul-Enein, A. A. Al-Badr, Anal. Profiles Drug Subs. 8, 351-370 (1979). Review of pharmacology and clinical experience: D. S. Cooper, N. Engl. J. Med. 311, 1353-1362 (1984).
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