
CAS Name: 1,3-Diphenyl-2-propen-1-one
Additional Names: chalkone; benzylideneacetophenone; benzalacetophenone; phenyl styryl ketone
Percent Composition: C 86.51%, H 5.81%, O 7.68%
Literature References: Prepd by the action of NaOH on an alcoholic soln of benzaldehyde and acetophenone: E. P. Kohler, H. M. Chadwell, Org. Synth. coll. vol. I, 78 (1941).
CAS Name: N,4-Dimethyl-N-nitrosobenzenesulfonamide
Additional Names: N-methyl-N-nitroso-p-toluenesulfonamide
Trademarks: Diazald (Aldrich)
Percent Composition: C 44.85%, H 4.70%, N 13.08%...
Literature References: Prepd by the action of nitrous acid on p-tolylsulfonylmethylamide: DE 224388 (1910 to Bayer); Frdl. 10, 1216; Chem. Zentralbl. 1910, II, 609; Takizawa, J. Pharm. Soc. Jpn. 70, 490 (1950); de Boer, Backer, Rec. Trav. Chim. 73, 229 (1954); Org. Synth. 34, 96 (1954).
CAS Name: 4-(Acetylamino)benzenesulfonic acid
Additional Names: N-p-acetylanilinosulfonic acid; acetanilidsulfonic acid; 4-acetamidobenzenesulfonic acid
Percent Composition: C 44.64%, H 4.21...
Literature References: Prepd by the action of oleum or sulfuric acid on acetanilide in acetic anhydride: Junghahn, Neumann, Ber. 33, 1366 (1900); Söll, Stutzer, Ber. 42, 4539 (1909).
CAS Name: Oxiranemethanol
Additional Names: 2,3-epoxy-1-propanol; 3-hydroxypropylene oxide
Percent Composition: C 48.64%, H 8.16%, O 43.19%
Literature References: Prepd by the action of perbenzoic acid on allyl alc: Prileshajew, Ber. 42, 4813 (1909); from glycerol-1-monochlorohydrin by the action of KOH in alc, or by the action of sodium in ether: Rider, Hill, J. Am. Chem. Soc. 52, 1521 (1930). L-form prepd from L-1-(p-toluenesulfonyl)glycerol: Sowden, Fischer, ibid. 64, 1291 (1942). Acute toxicity data: E. D. Thompson, R. A. Hiles, Food Cosmet. Toxicol. 19, 347 (1981); E. D. Thompson, D. P. Gibson, Food Chem. Toxicol. 22, 665 (1984).
CAS Name: Triphenylmethanol
Additional Names: tritanol
Percent Composition: C 87.66%, H 6.19%, O 6.15%
Literature References: Prepd by the action of phenylmagnesium bromide on benzophenone: Acree, Ber. 37, 2755 (1904); Peters et al., J. Am. Chem. Soc. 47, 452 (1925); Dubsky, Jacot-Guillarmod, Helv. Chim. Acta 53, 1965 (1970); by the action of potassium permanganate on triphenylfluoro- or triphenylchloromethane: Blicke, J. Am. Chem. Soc. 46, 1518 (1924). Convenient lab prepn from methyl benzoate and phenylmagnesium bromide: L. F. Fieser, Experiments in Organic Chemistry (Boston, 3rd ed., 1955) p 77.
Additional Names: Carbonic acid bis(2-methoxyphenyl) ester; guaiacol carbonic acid neutral ester; carbonic acid guaiacol ether
Trademarks: Duotal
Percent Composition: C 65.69%, H 5.14%, O 29...
Literature References: Prepd by the action of phosgene on a concd soln of guaiacol in aq NaOH: DE 58129 (to Bayer); S. P. Schotz, Synthetic Organic Compounds (London, 1925) p 137; J. Schwyzer, Die Fabrikation pharmazeutischer und chemisch-technischer Produkte (Berlin, 1931) p 212; H. P. Kaufmann, Arzneimittel-Synthese (Springer-Verlag, 1953) p 607.
CAS Name: N,N-Diethylisonicotinamide
Additional Names: pyridine-4-carboxylic acid diethylamide
Percent Composition: C 67.39%, H 7.92%, N 15.72%, O 8.98%
Literature References: Prepd by the action of phosphorus oxychloride upon a mixture of isonicotinic acid and diethylamine: Carrara, US 2858317 (1958 to Lepetit).
CAS Name: N,N-Bis(2-chloroethyl)benzenamine
Additional Names: N,N-bis(2-chloroethyl)aniline; phenylbis[2-chloroethylamine]; b,b'-dichlorodiethylaniline
Percent Composition: C 55.06%, H 6.01%...
Literature References: Prepd by the action of phosphorus pentachloride on N,N-bis-[2-hydroxyethyl]aniline (phenyldiethanolamine): Robinson, Watt, J. Chem. Soc. 1934, 1538; Korshak, Strepikheev, J. Gen. Chem. USSR 14, 312 (1944).
CAS Name: Methanethioamide
Percent Composition: C 19.65%, H 4.95%, N 22.92%, S 52.47%
Literature References: Prepd by the action of phosphorus pentasulfide on formamide: Willstätter, Wirth, Ber. 42, 1911 (1909). Synthesis: Erlenmeyer, Menzi, Helv. Chim. Acta 31, 2071 (1948); Schmitz, US 2682558 (1954 to du Pont); R. Tull, L. M. Weinstock, Angew. Chem. Int. Ed. 8, 278 (1969). Spectroscopic studies: R. Sugisaki et al., J. Mol. Spectrosc. 49, 241 (1974); R. H. Judge et al., Can. J. Chem. 65, 2100 (1987). Use in synthesis of thiazoles: T. J. Cousineau, J. A. Secrist III, J. Org. Chem. 44, 4351 (1979); H. Fukatsu et al., Heterocycles 29, 1517 (1989).
CAS Name: 1,1',1'',1'''-(1,2-Ethanediyldinitrilo)tetrakis[2-propanol]
Additional Names: 1,1',1'',1'''-(ethylenedinitrilo)tetra-2-propanol; N,N,N',N'-tetrakis(2-hydroxypropyl)ethylenediamine
...
Literature References: Prepd by the action of propylene oxide on ethylenediamine: Lundsted, Schulz, US 2697118 (1954 to Wyandotte).
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