
Additional Names: O,O-Succinyldicholine iodide; diacetylcholine iodide; diacetylcholine diiodide; suxamethonium iodide; bis(b-dimethylaminoethyl)succinate bis(methyl iodide)
Trademarks: Celocur...
Literature References: Prepd by reacting b-bromoethyl succinate with trimethylamine: Glick, J. Biol. Chem. 137, 357 (1941); Fusco et al., Gazz. Chim. Ital. 79, 129, 837 (1949); Walker, J. Chem. Soc. 1950, 193. Succinic acid chloride may be coupled with choline chloride directly or with dimethylaminoethanol, followed by quaternization with methyl iodide: Tammelin, Acta Chem. Scand. 7, 185 (1953). A third method is to start with the diethyl ester of succinic acid, then bring about the exchange reaction with dimethylaminoethanol, and quaternize with methyl iodide: Phillips, J. Am. Chem. Soc. 71, 3264 (1949).
CAS Name: Tripotassium hexakis(cyano-C)cobaltate(3-)
Additional Names: potassium cyanocobaltate(III); potassium cobalticyanide; potassium cobaltihexacyanide; cobalt potassium cyanide
Percent...
Literature References: Prepd by reacting cobalt acetate or cyanide with potassium cyanide, followed by air-oxidation of the cobaltocyanide formed: Biltz, Biltz, Z. Anorg. Allg. Chem. 50, 108 (1906); Grube, Z. Elektrochem. 32, 561 (1926); Benedetti-Pichler, Z. Anal. Chem. 70, 258 (1927); Bigelow, Inorg. Synth. 2, 225 (1946).
CAS Name: Chloroacetic acid 1,1-dimethyl ester
Additional Names: t-butyl chloroacetate; chloroacetic acid tert-butyl ester
Percent Composition: C 47.85%, H 7.36%, Cl 23.54%, O 21.25%
Literature References: Prepd by reacting monochloroacetic acid and isobutylene in dioxane in the presence of sulfuric acid: Johnson et al., J. Am. Chem. Soc. 75, 4995 (1953); from tert-butyl alcohol, chloroacetyl chloride and dimethylaniline: Baker, Org. Synth. 24, 21 (1944).
CAS Name: 2-Methylbenzaldehyde
Additional Names: o-toluylaldehyde
Percent Composition: C 79.97%, H 6.71%, O 13.32%
Literature References: Prepd by reacting nitropropane with o-xylyl bromide in the presence of sodium ethanoate: Hass, Bender, Org. Synth. 30, 99 (1950).
CAS Name: 2-Methylbenzamide
Percent Composition: C 71.09%, H 6.71%, N 10.36%, O 11.84%
Literature References: Prepd by reacting o-tolunitrile, hydrogen peroxide, 95% alcohol, and sodium hydroxide at 40-50°: Noller, Org. Synth. coll. vol. II, 586 (1943). Also prepared by reacting the nitrile with boron fluoride in dil acetic acid: Hauser, Hoffenberg, J. Org. Chem. 20, 1448 (1955).
CAS Name: N'-(4-Chlorophenyl)-N,N-dimethylurea
Additional Names: 1,1-dimethyl-3-(p-chlorophenyl)urea; CMU
Trademarks: Karmex Monuron Herbicide; Telvar (DuPont)
Percent Composition: C 54.4...
Literature References: Prepd by reacting p-chlorophenyl isocyanate with dimethylamine: Bucha, Todd, Science 114, 493 (1951); see also US 2655444; US 2655445; US 2655446; US 2655447. Toxicity study: G. W. Bailey, J. L. White, Residue Rev. 10, 97 (1965). Review: McCall, Agric. Chem. 7, 40 (1952).
CAS Name: a-Phenyl-1-piperidineacetic acid 2-(diethylamino)ethyl ester
Additional Names: b-diethylaminoethyl phenylpiperidinoacetate; b-diethylaminoethyl a-(1-piperidyl)phenylacetate
Percent...
Literature References: Prepd by reacting piperidine with phenylchloroacetic acid ethyl ester in chloroform: Reetz, DE 859892 (1952 to Nordmark-Werke); from b-diethylaminoethyl phenylbromoacetate and piperidine in chloroform: Blicke et al., J. Am. Chem. Soc. 76, 3161 (1954); from ethyl a-(1-piperidyl)phenylacetate and b-diethylaminoethyl chloride: Moffett, Hart, J. Am. Pharm. Assoc. Sci. Ed. 42, 717 (1953). Clinical tests: Ciravegna et al., Clin. Ter. 57, 227 (1971).
CAS Name: 5-[(3-Carboxy-4-hydroxyphenyl)(3-carboxy-4-oxo-2,5-cylohexadien-1-ylidene)methyl]-2-hydroxybenzoic acid triammonium salt
Additional Names: 3-[bis(3-carboxy-4-hydroxyphenyl)methylene]-...
Literature References: Prepd by reacting sodium nitrite with salicylic acid and adding formaldehyde, then treating with ammonia: G. B. Heisig, W. M. Lauer, Org. Synth. coll. vol. I, 54 (2nd ed., 1941).
CAS Name: 1,1',1''-(1-Chloro-1-ethenyl-2-ylidene)tris[4-methoxybenzene]
Additional Names: chlorotris(p-methoxyphenyl)ethylene; tri-p-anisylchloroethylene; tris(p-methoxyphenyl)chloroethylene
CAS Name: a-[(1-Methyl-2-phenylethyl)amino]benzeneacetonitrile
Additional Names: N-(a-methylphenethyl)-2-phenylglycinonitrile; a-phenyl-a-(b-phenylisopropylamino)acetonitrile; a-phenyl-a-(1-met...
Literature References: Prepd by reaction of DL-b-phenylisopropylamine with sodium cyanide and benzaldehyde or with a-phenyl-a-bromoacetonitrile: Klosa, DE 1112987 (1959), C.A. 56, 3409d (1962); idem, J. Prakt. Chem. 20, 275 (1963). Pharmacology: Dominok, Oelssner, Acta Biol. Med. Ger. 20, 625 (1968); Beyer et al., Dtsch. Apoth. Ztg. 111, 677, 680 (1971). Metabolic studies: Remberg et al., Arch. Toxicol. 29, 153 (1972). Chemistry: Beyrich et al., Pharmazie 27, 28 (1972); Gloeckl, Beyrich, ibid. 95.
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