
CAS Name: 4-Hydroxy-3-nitrophenylarsonic acid
Additional Names: 4-hydroxy-3-nitrobenzenearsonic acid; 3-nitro-4-hydroxyphenylarsonic acid; 2-nitro-1-hydroxybenzene-4-arsonic acid; nitrophenolar...
Literature References: Prepd by treating sodium p-hydroxyphenylarsonate with a mixture of nitric and sulfuric acids at 0°: Benda, Bertheim, Ber. 44, 3446 (1911); DE 224953 C.A. 5, 156 (1911). Toxicity study: Kerr et al., Toxicol. Appl. Pharmacol. 5, 507 (1963). Review of toxicology and human exposure: Toxicological Profile for Arsenic (PB2000-108021, 2000) 468 pp.
Percent Composition: O 25.76%, Se 42.38%, Sn 31.86%
Literature References: Prepd by treating stannic oxide with selenious acid: Berzelius, cited in Mellor's vol. X, 832 (1930).
CAS Name: 1-Phenyl-2,5-pyrrolidinedione
Additional Names: N-phenylsuccinimide; N-phenylbutanimide
Percent Composition: C 68.56%, H 5.18%, N 8.00%, O 18.27%
Literature References: Prepd by treating succinanilic acid with acetyl chloride: Ruggli, Ann. 412, 4 (1916); Warren, Briggs, Ber. 64, 29 (1931); L. F. Fieser, Experiments in Organic Chemistry (Boston, 1955) p 106.
CAS Name: 3-Indoleethanol
Additional Names: 3-w-hydroxyethylindole; 2-(3-indolyl)ethyl alcohol; 2-indolyl(3)-ethanol; b-indolylethyl alcohol; 3-b-hydroxyethylindole
Percent Composition: C 74...
Literature References: Prepd by treatment of indolemagnesium bromide with ethylene oxide: Oddo, Cambieri, Gazz. Chim. Ital. 60, 19 (1939); Snyder, Pilgrim, J. Am. Chem. Soc. 70, 1962 (1948); by Bouveault-Blanc reduction of 3-indoleacetic ester: Jackson, J. Biol. Chem. 88, 659 (1930); by treatment of indolemagnesium iodide with ethylene chlorohydrin: Majima, Hoshino, Ber. 58, 2042 (1925); from gramine: Snyder, Pilgrim, J. Am. Chem. Soc. 70, 3770 (1948). By lithium aluminum hydride reduction of methyl 3-indoleglycolate: Speeter, Anthony, US 3076814 (1963 to Upjohn).
CAS Name: Tripotassium tris(ethanedioato)chromate(3-)
Additional Names: tripotassium tris(oxalato)chromate(3-); potassium trioxalatochromate(III); potassium chromic oxalate
Percent Compositi...
Literature References: Prepd by treatment of oxalic acid and K2C2O4 with K2Cr2O7: Bailar, Jr., Jones, Inorg. Synth. 1, 37 (1939); Hein, Herzog in Handbook of Preparative Inorganic Chemistry vol. 2, G. Brauer, Ed. (Academic Press, New York, 2nd ed., 1965) p 1372.
CAS Name: 2-Methyl-2-propenenitrile
Additional Names: isopropenylnitrile; a-methylacrylonitrile; isopropene cyanide
Percent Composition: C 71.61%, H 7.51%, N 20.88%
Literature References: Prepd by vapor-phase catalytic oxidation of methallylamine: Peters et al., Ind. Eng. Chem. 40, 2046 (1948); US 2375016 (1945 to Shell); by the dehydration of methacrylamide: Kung, US 2373190 (1945 to Goodrich); from isopropylene oxide and ammonia: Spillane, Kayser, US 2557703 (1951 to Allied Chem.). Toxicity study: Smyth et al., Am. Ind. Hyg. Assoc. J. 23, 95 (1962).
Percent Composition: P 20.73%, Se 79.27%
Literature References: Prepd by warming a mixture of phosphorus and selenium in the correct proportions: Hahn, J. Prakt. Chem. [1] 93, 430 (1864); Muthmann, Clever, Z. Anorg. Chem. 13, 191 (1897); Meyer, ibid. 30, 258 (1902); 61B, 1807 (1928).
CAS Name: 1-Carboxy-N,N,N-trimethylmethanaminium inner salt compd with 2,2,2-trichloro-1,1-ethanediol (1:1)
Trademarks: Beta-Chlor (Mead Johnson); Somilan (BDH)
Percent Composition: C 29.76%...
Literature References: Prepd by warming betaine hydrate and chloral hydrate: Petrow et al., GB 874246 (1959 to British Drug Houses).
CAS Name: N-Acetylglycine
Additional Names: acetamidoacetic acid; acetylaminoacetic acid; acetylglycocoll; ethanoylaminoethanoic acid
Percent Composition: C 41.03%, H 6.03%, N 11.96%, O 40.9...
Literature References: Prepd by warming glycine with a slight excess of acetic anhydride in benzene: Radenhausen, J. Prakt. Chem. [2] 52, 437 (1895); by warming glycine in glacial acetic acid with the stoichiometric amount of acetic anhydride: Dakin, J. Biol. Chem. 82, 443 (1929).
CAS Name: N-Hydroxybenzenamine
Additional Names: b-phenylhydroxylamine; N-phenylhydroxylamine
Percent Composition: C 66.04%, H 6.47%, N 12.83%, O 14.66%
Literature References: Prepd by zinc reduction of nitrobenzene in ammonium chloride soln: Kamm, Org. Synth. 4, 57 (1925).
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