
Additional Names: Mannitol nitrate; nitromannite; nitromannitol
Trademarks: Medemanol; Dilangil; Moloid (Sámedica); Mannitrin; Manexin
Percent Composition: C 15.94%, H 1.78%, N 18.59%, O 63....
Literature References: Made by nitration of mannitol: Fleury et al., Mem. Poudres 31, 107 (1949).
CAS Name: 4-Heptanone
Additional Names: butyrone
Percent Composition: C 73.63%, H 12.36%, O 14.01%
Literature References: Made by passing butyric acid over precipitated CaCO3 at 450°.
CAS Name: 1,2-Benzenediamine
Additional Names: o-diaminobenzene
Percent Composition: C 66.64%, H 7.46%, N 25.90%
Literature References: Made by reducing o-nitroaniline with Zn and NaOH.
CAS Name: N-Methyl-N-phenylacetamide
Additional Names: acetomethylanilide
Trademarks: Exalgin
Percent Composition: C 72.46%, H 7.43%, N 9.39%, O 10.72%
Literature References: Made by the action of acetic anhydride on methylaniline.
CAS Name: Butanediamide
Percent Composition: C 41.37%, H 6.94%, N 24.12%, O 27.56%
Literature References: Made by the action of ammonia water on the dimethyl or diethyl ester of succinic acid.
CAS Name: Phenylcarbamic acid ethyl ester
Additional Names: ethyl phenylcarbamate; ethyl carbanilate
Percent Composition: C 65.44%, H 6.71%, N 8.48%, O 19.37%
Literature References: Made by the action of aniline on ethyl chloroformate.
CAS Name: 2-Hydroxybenzoic acid phenyl ester
Trademarks: Salol
Percent Composition: C 72.89%, H 4.71%, O 22.41%
Literature References: Made by the action of phosphorus oxychloride on a mixture of phenol and salicylic acid.
CAS Name: 2,4-Pentanedione
Additional Names: diacetylmethane
Percent Composition: C 59.98%, H 8.05%, O 31.96%
Literature References: Made by the action of sodium on ethyl acetate and acetone or by the action of anhydrous aluminum chloride on acetyl chloride in the presence of an inert solvent: Combes, Compt. Rend. 103, 814 (1886); Ann. Chim. (Paris) 12, 199 (1887); Claisen, Ber. 38, 695 (1905); Hunt, US 2737528 (1956 to Shawinigan Chem.); Georgieff, US 2834811 (1958); Gattermann-Wieland, Praxis des Organischen Chemikers (de Gruyter, Berlin, 40th ed, 1961) p 219. Toxicity data: Carpenter, J. Ind. Hyg. Toxicol. 31, 343 (1949).
CAS Name: 4-Chloro-5-methyl-2-(1-methylethyl)phenol
Additional Names: 6-chlorothymol; 4-chlorothymol; 1-methyl-3-hydroxy-4-isopropyl-6-chlorobenzene; 6-chloro-4-isopropyl-1-methyl-3-phenol
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Literature References: Made by the action of sulfuryl chloride on thymol in CCl4: Satriana et al., J. Am. Pharm. Assoc. 39, 135 (1950); H. Pahlicke, DE 905738 (1954 to Diwag), C.A. 52, 16294i (1958). Antifungal properties: M. Iannarone, Drug Stand. 25, 190 (1957).
CAS Name: 1,8-Naphthalenedicarboxylic acid
Percent Composition: C 66.67%, H 3.73%, O 29.60%
Literature References: Made by the oxidation of acenaphthene with chromic acid mixture, etc.: Graebe, Gfeller, Ber. 25, 652 (1895); Ogilvie, Wilder, US 2379032 (1945 to Allied Chem.); Karishin, Fedorenko, Zh. Prikl. Khim. 29, 955 (1956), C.A. 50, 14677b (1956).
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