
CAS Name: 1-Ethyl-1H-pyrrole-2,5-dione
Percent Composition: C 57.59%, H 5.64%, N 11.19%, O 25.57%
Literature References: Prepd by heating N-ethylmaleamic acid in paraffin: Marrian, J. Chem. Soc. 1949, 1515.
CAS Name: 2-Mercaptobenzoic acid
Additional Names: o-sulfhydrylbenzoic acid
Percent Composition: C 54.53%, H 3.92%, O 20.75%, S 20.80%
Literature References: Prepd by heating o-halogenated benzoic acids with an alkaline hydrosulfide in the presence of copper: DE 189200 (1906); by reduction of dithiosalicylic acid: Claasz, Ber. 45, 2427 (1912); DE 205450; C. F. H. Allen, D. D. MacKay, Org. Synth. coll. vol. II, 580 (1943).
CAS Name: 2,2'-[[[4-[(Aminocarbonyl)amino]phenyl]arsinidene]bis(thio)]bis[benzoic acid]
Additional Names: (p-ureidophenylarsylenedithio)di-o-benzoic acid; (p-ureidobenzenearsylenedithio)di-o-be...
Literature References: Prepd by heating o-HSC6H4COOH and Carbarsone oxide in aq alkali, purified by repeated precipitation with acid and dissolving in alkali: Rohrmann, US 2516831 (1950 to Lilly). Compare Arsenamide, Thiocarbarsone, Carbarsone.
CAS Name: N-[Bis(4-methoxyphenyl)methylene]benzenemethanamine
Percent Composition: C 79.73%, H 6.39%, N 4.23%, O 9.66%
Literature References: Prepd by heating p,p¢-dimethoxybenzophenone, thionyl chloride and benzylamine: Schönberg, Urban, Ber. 67, 1999 (1934).
CAS Name: 4-(1,1-Dimethylethyl)phenol
Additional Names: butylphen
Percent Composition: C 79.95%, H 9.39%, O 10.65%
Literature References: Prepd by heating phenol with isobutanol in the presence of zinc chloride: DE 17311; Frdl. 1, 22; also from phenol, tert-butyl chloride and excess alkali in alcohol: Lewis, J. Chem. Soc. 83, 329 (1903). See also Smith, J. Am. Chem. Soc. 55, 3718 (1933); Natelson, ibid. 56, 1583 (1934); Huston, Hsieh, ibid. 58, 439 (1936); US 2039344 (1936 to Dow); Isagulyants, Bagryantseva, C.A. 33, 8183 (1939). Toxicity study: H. F. Smyth et al., Am. Ind. Hyg. Assoc. J. 30, 470 (1969).
CAS Name: 1-Bromo-4-isocyanatobenzene
Additional Names: 4-bromophenylcarbimide; p-bromophenylcarbonimide; p-bromocarbanil
Percent Composition: C 42.46%, H 2.04%, Br 40.35%, N 7.07%, O 8.08%
Literature References: Prepd by heating phenyl isocyanate dibromide: Curtius, J. Prakt. Chem. 87, 517 (1913); by distilling p-bromophenylurethan and P2O5: Dennstedt, Ber. 13, 228 (1880).
CAS Name: p-Aminobenzenesulfonyl fluoride
Percent Composition: C 41.14%, H 3.45%, F 10.85%, N 8.00%, O 18.27%, S 18.30%
Literature References: Prepd by heating potassium fluoride with 4-acetamidobenzenesulfonyl chloride: Parker, Hofmann, US 2576037 (1951 to Am. Cyanamid).
CAS Name: 5,6,6a,7-Tetrahydro-10-methoxy-6-methyl-4H-dibenzo[de,g]quinoline-2,11-diol
Additional Names: 10-methoxyaporphine-2,11-diol; 2,11-dihydroxy-10-methoxyaporphine
Percent Composition:...
Literature References: Prepd by heating thebaine with HCl. Formation from bulbocapnine: Ayer, Taylor, J. Chem. Soc. 1956, 472. Review: Small, Lutz, "Chemistry of the Opium Alkaloids" in U.S. Public Health Reports Suppl. No. 103 (Washington, 1932); R. H. F. Manske, H. L. Holmes, The Alkaloids vol. II (Academic Press, New York, 1952) pp 112-116.
CAS Name: N-(Aminocarbonyl)-2-bromo-2-ethylbutanamide
Additional Names: (a-bromo-a-ethylbutyryl)urea; (a-bromo-a-ethylbutyryl)carbamide; bromodiethylacetylurea; bromodiethylacetylcarbamide
T...
Literature References: Prepd by heating urea (to ~50°) with a-bromo-a-ethylbutyryl bromide (C2H5)2CBrCOBr, see DE 225710 (1910); Frdl. 10, 1160; Chem. Zentralbl. 1910, II, 1008. Patent literature: Slotta, Grundriss der modernen Arzneistoff-Synthese (Stuttgart, 1931); H. P. Kaufmann, Arzneimittel-Synthese (Berlin, 1953).
CAS Name: 2,5,8,11-Tetraoxadodecane
Additional Names: triethylene glycol dimethyl ether
Percent Composition: C 53.91%, H 10.18%, O 35.91%
Literature References: Prepd by high pressure hydrogenation of 1,1,2,2-tetrakis(2-methoxyethoxy)ethane: McNamee, MacDowell, US 2425042 (1947 to Carbide Carbon Chem.).
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