
Additional Names: 4-Dimethylaminobenzenecarbonal; Ehrlich's reagent
Percent Composition: C 72.46%, H 7.43%, N 9.39%, O 10.72%
Literature References: Prepd by formylation of dimethylaniline with dimethylformamide: Campaigne, Archer, Org. Synth. coll. vol. IV, 331 (1963).
CAS Name: N-(2,6-Dimethyl-4-pyrimidinyl)-4-(formylamino)benzenesulfonamide
Additional Names: 4'-[(2,6-dimethyl-4-pyrimidinyl)sulfamoyl]formanilide; N-[4-[[(2,6-dimethyl-4-pyrimidinyl)amino]sulf...
Literature References: Prepd by formylation of sulfisomidine: Brand, Rieckhoff, DE 1122511; DE 1126857 (both 1962 to VEB Farbenfabrik Wolfen).
CAS Name: Phthalic acid potassium acid salt
Additional Names: potassium acid phthalate; potassium hydrogen phthalate; acid potassium phthalate
Percent Composition: C 47.05%, H 2.47%, K 19.15...
Literature References: Prepd by half-neutralization of a phthalic anhydride soln: F. J. Welcher, Organic Analytical Reagents vol. 2 (Van Nostrand, New York, 1947) pp 75-79.
CAS Name: 2-Hydroxypropanoic acid methyl ester
Percent Composition: C 46.15%, H 7.75%, O 46.11%
Literature References: Prepd by heating 1 mole lactic acid condensation polymer with 2.5-5 moles of methanol and a small quantity of H2SO4 at 100° for 1-4 hours in a heavy-walled bottle: Rehberg, Org. Synth. coll. vol. III, 47-48 (1955).
CAS Name: 1,1'-Iminobis-9,10-anthracenedione
Additional Names: 1,1'-iminodianthraquinone; dianthraquinonylamine; dianthrimide
Percent Composition: C 78.31%, H 3.52%, N 3.26%, O 14.90%
Literature References: Prepd by heating 1-aminoanthraquinone with 1-chloroanthraquinone in nitrobenzene in the presence of copper: Bayer Co., DE 162823; Chem. Zentralbl. 1905, II, 1206; Eckert, Steiner, Monatsh. Chem. 35, 1129 (1914); FIAT Report no. 1313, vol. II (1948), p 137.
CAS Name: 5-(2-Bromo-2-propenyl)-1-methyl-5-(1-methylethyl)-2,4,6(1H,3H,5H)-pyrimidinetrione
Additional Names: 5-(2-bromoallyl)-5-isopropyl-1-methylbarbituric acid; N-methyl-b-bromoallylisoprop...
Literature References: Prepd by heating 5-isopropyl-1-methylbarbituric acid with 2,3-dibromo-1-propene in alkaline soln: Boedecker, Gruber, DE 613403 (1937 to Riedel de Haen). See also DE 627380; US 2080071.
CAS Name: N,N-Dimethyl-N'-2-pyridinyl-N'-(2-thienylmethyl)-1,2-ethanediamine
Additional Names: 2-[(2-dimethylaminoethyl)-2-thenylamino]pyridine; N,N-dimethyl-N'-(2-pyridyl)-N'-(2-thenyl)ethylen...
Literature References: Prepd by heating a 2-thenyl halide with an alkali metal salt of N,N-dimethyl-N¢-(2-pyridyl)ethylenediamine: Kyrides, US 2581868 (1952 to Monsanto). Alternate syntheses: Weston, J. Am. Chem. Soc. 69, 980 (1947); Clapp et al., ibid. 1549. Toxicity data: H. M. Lee et al., Proc. Soc. Exp. Biol. Med. 80, 458 (1952). Carcinogenicity study: W. Lijinsky et al., Science 209, 817 (1980). Study of mechanism of hepatocarcinogenicity: K. L. Steinmetz et al., Carcinogenesis 9, 959 (1988). Clinical pharmacokinetics: E. P. Calandre et al., Clin. Pharmacol. Ther. 29, 527 (1981). HPLC determn in feed and sleep aid tablets: B. Shaikh, M. R. Hallmark, J. Assoc. Off. Anal. Chem. 64, 889 (1981); in feed, urine and wastewater: H. C. Thompson, Jr., C. L. Holder, J. Chromatogr. 283, 251 (1984).
CAS Name: 3-(3-Nitrophenyl)-2-propenoic acid
Percent Composition: C 55.96%, H 3.65%, N 7.25%, O 33.13%
Literature References: Prepd by heating a mixture of m-nitrobenzaldehyde, sodium acetate and acetic anhydride: Thayer, Org. Synth. 5, 83 (1925). From m-nitrobenzaldehyde and malonic acid in the presence of glycine in a little water at 100°: Dakin, J. Biol. Chem. 7, 54 (1909-1910).
CAS Name: 7H-Benz[de]anthracen-7-one
Percent Composition: C 88.67%, H 4.38%, O 6.95%
Literature References: Prepd by heating a reduction product of anthraquinone with sulfuric acid and glycerol: Macleod, Allen, Org. Synth. 14, 4 (1934); cf. US 1626392 (1927). Review of toxicology: G. B. Singh et al., J. Sci. Ind. Res. 49, 288-296 (1990).
CAS Name: [4-[(2-Amino-2-oxoethyl)amino]phenyl]arsonic acid monosodium salt
Additional Names: N-(carbamoylmethyl)arsanilic acid monosodium salt; monosodium N-phenylglycinamide-p-arsonate
Tra...
Literature References: Prepd by heating a soln of arsanilic acid in aq NaOH, Na2CO3 and chloroacetamide: Jacobs, Heidelberger, J. Am. Chem. Soc. 41, 1590 (1919); Org. Synth. 8, 100 (1928). US 1280119; US 1280124; US 1280126 (1918); US 2465308 (1949).
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