
CAS Name: 2,6-DichlorobenzonitrileTrademarks: Casoron (Solvay Duphar)
Percent Composition: C 48.88%, H 1.76%, Cl 41.22%, N 8.14%
Literature References: Prepn: Reich, Bull. Soc. Chim. Fr. [4] 21, 217 (1917); Norris, Klemka, J. Am. Chem. Soc. 62, 1432 (1940); Chang et al., C.A. 53, 6134d (1959); Koopman, Rec. Trav. Chim. 80, 1075 (1961); Hackmann, ten Haken GB 861899; Higson, GB 862937 (both 1961 to Shell). Use as herbicide: Koopman, Daams, US 3027248 (1962 to N. A. Phillips). Fate in crops, soil and animals: Beynon, Wright, Residue Rev. 43, 23 (1972); Veroop, ibid. 55. Toxicity data: G. W. Bailey, J. L. White, ibid. 10, 97 (1965).
CAS Name: 2,6-DichlorobenzonitrileTrademarks: Casoron (Solvay Duphar)
Percent Composition: C 48.88%, H 1.76%, Cl 41.22%, N 8.14%
Literature References: Prepn: Reich, Bull. Soc. Chim. Fr. [4] 21, 217 (1917); Norris, Klemka, J. Am. Chem. Soc. 62, 1432 (1940); Chang et al., C.A. 53, 6134d (1959); Koopman, Rec. Trav. Chim. 80, 1075 (1961); Hackmann, ten Haken GB 861899; Higson, GB 862937 (both 1961 to Shell). Use as herbicide: Koopman, Daams, US 3027248 (1962 to N. A. Phillips). Fate in crops, soil and animals: Beynon, Wright, Residue Rev. 43, 23 (1972); Veroop, ibid. 55. Toxicity data: G. W. Bailey, J. L. White, ibid. 10, 97 (1965).
CAS Name: Androst-4-ene-3,11,17-trione
Additional Names: Reichstein's substance G
Percent Composition: C 75.97%, H 8.05%, O 15.98%
Literature References: Prepn: Reichstein, Helv. Chim. Acta 19, 29, 1107 (1936); Kendall et al., J. Biol. Chem. 116, 267 (1936); Reichstein, Helv. Chim. Acta 20, 817, 953 (1937). Total synthesis: Velluz et al., Compt. Rend. 250, 1293 (1960). Crystal structure: Ohrt et al., Acta Crystallogr. 19, 479 (1965). Metabolism: Bradlow et al., Steroids 10, 233 (1967).
CAS Name: 2-(2-Butoxyethoxy)ethanol
Additional Names: diethylene glycol monobutyl ether; butyl digol
Trademarks: Butyl Diicinol (ICI)
Percent Composition: C 59.23%, H 11.18%, O 29.59%
Literature References: Prepn: Riemschneider, Gross, Monatsh. Chem. 90, 783 (1959). Purification: Miller, Yonan, J. Am. Chem. Soc. 79, 5931 (1957); Ridley, Ridley, GB 795866 (1958 to Esso). Toxicity data: Smyth et al., J. Ind. Hyg. Toxicol. 23, 259 (1941).
CAS Name: 2,3-Bis(acetyloxy)benzoic acid
Additional Names: o-pyrocatechuic acid diacetate; diacetylpyrocatechol-3-carboxylic acid; 2,3-diacetoxybenzoic acid
Trademarks: Movirene; Artromialgi...
Literature References: Prepn: Rietz, US 1140716 (1914); Simokoriyama, Bull. Chem. Soc. Jpn. 16, 284 (1941).
CAS Name: N,N-Dimethyl-2-[(4-methylphenyl)phenylmethoxy]ethanamine
Additional Names: N,N-dimethyl-2-[(p-methyl-a-phenylbenzyl)oxy]ethylamine; b-dimethylaminoethyl 4-methylbenzhydryl ether; p-me...
Literature References: Prepn: Rieveschl, US 2527962 (1950 to Parke, Davis); GB 683483 (1952 to Fabriken Brocades-Stheeman Pharmacia).
CAS Name: 2-[(4-Bromophenyl)phenylmethoxy]-N,N-dimethylethanamine
Additional Names: 2-(p-bromo-a-phenylbenzyloxy)-N,N-dimethylethylamine; b-(p-bromobenzhydryloxy)ethyldimethylamine; b-dimethyla...
Literature References: Prepn: Rieveschl, US 2527963 (1950 to Parke, Davis).
Percent Composition: Fe 62.15%, H 2.24%, O 35.61%
Literature References: Prepn: Rihl, Fricke, Z. Anorg. Allg. Chem. 251, 406 (1943); Leussing, Kolthoff, J. Am. Chem. Soc. 75, 2476 (1953). Oxidation products: Feitknecht, Keller, Z. Anorg. Chem. 262, 61 (1950); Mayne, J. Chem. Soc. 1953, 129; Shipko, Douglas, J. Phys. Chem. 60, 1519 (1956).
CAS Name: 17-(Acetyloxy)-6-chloropregna-1,4,6-triene-3,20-dione
Additional Names: 6-chloro-17-hydroxypregna-1,4,6-triene-3,20-dione acetate; 1,6-bisdehydro-6-chloro-17a-acetoxyprogesterone; D1-...
Literature References: Prepn: Ringold et al., J. Am. Chem. Soc. 81, 3485 (1959); GB 890315 (1962 to Upjohn), C.A. 57, 5996c (1962); 76, 14813y (1972); Campbell, Babcock, DE 1243682 (1967 to Upjohn), C.A. 67, 100343r (1967). Activity studies: Dorfman, Kincl, Steroids 1, 185 (1963); Weichert et al., Arzneim.-Forsch. 17, 1103 (1967); Gerber et al., J. Small Anim. Pract. 14, 151 (1973).
CAS Name: 4-Chloro-6-[(3-hydroxy-2-butenylidene)amino]-N1-2-propenyl-1,3-benzenedisulfonamide
Additional Names: N'-allyl-4-chloro-6-[(3-hydroxy-2-butenylidene)amino]-m-benzenedisulfonamide; 2-(...
Literature References: Prepn: Robertson, FR 1331680 (1963 to Lakeside), corresp to US 3188329 (1965 to Colgate-Palmolive); Robertson et al., J. Med. Chem. 8, 90 (1965).
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