
CAS Name: 1-Chloro-2,5-pyrrolidinedione
Additional Names: succinchlorimide
Percent Composition: C 35.98%, H 3.02%, Cl 26.55%, N 10.49%, O 23.96%
Literature References: Prepn from succinimide: Hirst, Macbeth, J. Chem. Soc. 121, 2169 (1922); Zimmer, Audrieth, J. Am. Chem. Soc. 76, 3856 (1954). Crystal structure: Brown, Acta Crystallogr. 9, 193 (1956); 14, 711 (1961). Toxicity data: Stohlman, Smith, Public Health Rep. 59, 541 (1944).
Percent Composition: C 49.56%, H 5.64%, O 44.80%
Literature References: Prepn from sucrose: Linstead et al., J. Am. Chem. Soc. 62, 3260 (1940). Synthesis: Lemieux, Huber, ibid. 78, 4117 (1956).
CAS Name: Trichloroethene
Additional Names: ethinyl trichloride
Trademarks: Tri-Clene (DuPont); Trilene (Zeneca); Trichloren; Algylen; Trimar; Triline; Trethylene; Westrosol; Chlorylen (Sche...
Literature References: Prepn from sym-tetrachloroethane by elimination of HCl (by boiling with lime): DE 171900; by passing tetrachloroethane vapor over CaCl2 catalyst at 300°: DE 263457; without catalyst at 450-470°: GB 575530 (1946 to du Pont). Physical properties: E. W. McGovern, Ind. Eng. Chem. 35, 1230 (1943); S. A. Mumford, J. W. C. Phillips, J. Chem. Soc. 1950, 75. Review of mfg processes: S. A. Miller, Chem. Process Eng. 47, 268 (1966); Faith, Keyes Clark's Industrial Chemicals, F. A. Lowenheim, M. K. Moran, Eds. (Wiley-Interscience, New York, 4th ed., 1975) pp 844-848. Toxicity data: H. S. Smyth et al., Am. Ind. Hyg. Assoc. J. 30, 470 (1969). Review of carcinogenic risk: IARC Monographs 20, 545-572 (1979); B. L. Van Duuren, Environ. Res. 49, 333 (1989). Review of use as anesthetic: J. V. Farman, Br. J. Anaesth. 53, Suppl. 3, 3S-9S (1981). Review of metabolism, toxicity and carcinogenicity: J. V. Bruckner et al., Crit. Rev. Toxicol. 20, 31-50 (1989); of toxicology and human exposure: Toxicological Profile for Trichloroethylene (PB98-101165, 1997) 335 pp. Series of articles on toxicology and risk assessment: Environ. Health Perspect. 108, Suppl. 2, 159-366 (2000).
CAS Name: (Z)-2,3-Dihydroxy-2-butenedioic acid
Additional Names: 1,2-dihydroxyethylenedicarboxylic acid
Percent Composition: C 32.45%, H 2.72%, O 64.83%
Literature References: Prepn from tartaric acid: Fenton, J. Chem. Soc. 87, 811 (1905); Nef, Ann. 357, 291 (1907).
Additional Names: Nitroform
Percent Composition: C 7.95%, H 0.67%, N 27.82%, O 63.56%
Literature References: Prepn from tetranitromethane and K4[Fe(CN)6] in aq soln: Chattaway, Harrison, J. Chem. Soc. 109, 171 (1916); by nitration of acetylene with nitric acid: Hager, Ind. Eng. Chem. 41, 2168 (1949).
CAS Name: 2,2'-Iminobis[benzoic acid]
Percent Composition: C 65.37%, H 4.31%, N 5.44%, O 24.88%
Literature References: Prepn from the alkali salts of anthranilic acid and of 2-chlorobenzoic acid in presence of copper: Ullmann, Ann. 355, 352 (1907).
CAS Name: 6-Hydroxy-2-naphthalenepropanoic acid
Additional Names: 2-hydroxy-6-naphthalenepropionic acid; amphihydroxynaphthyl-b-propionic acid
Percent Composition: C 72.21%, H 5.59%, O 22.20...
Literature References: Prepn from the corresponding methoxy compd: Jacques, Horeau, Bull. Soc. Chim. Fr. 1948, 714.
CAS Name: 7,8-Didehydro-4-hydroxy-3-methoxy-17-methylmorphinan-6-one
Additional Names: thebainone-A
Percent Composition: C 72.22%, H 7.07%, N 4.68%, O 16.03%
Literature References: Prepn from thebaine, codeinone or b-ethylthiocodide: Morris, Small, J. Am. Chem. Soc. 56, 2159 (1934). Earlier references and discussion of structure: Small, Lutz, "Chemistry of the Opium Alkaloids" in U.S. Public Health Reports Suppl. No. 103 (Washington, 1932). About anomalies in nomenclature and difference from metathebainone see Henry, Plant Alkaloids (London, 1939) p 249. Description of all thebainones: K. W. Bentley, The Chemistry of the Morphine Alkaloids (Oxford, 1954) p 219.
CAS Name: 1-Hexyl-3,7-dihydro-3,7-dimethyl-1H-purine-2,6-dione
Additional Names: 1-hexyltheobromine; 1-hexyl-3,7-dimethylxanthine; 3,7-dimethyl-1-hexyl-1H,3H-purin-2,6-dioneTrademarks: Cosaldon...
Literature References: Prepn from theobromine and hexyl halide: Eidebenz, Schuh, DE 860217 (1952 to Chem. Werke Albert); Serchi, Chimica 40, 451 (1964); Chkhikvadze et al., SU 202152 (1967), C.A. 69, 19368x (1968). Pharmacology: Cugurra, Echinard-Garin, Arch. Int. Pharmacodyn. Ther. 123, 481 (1960); Ramos et al., ibid. 153, 430 (1965); Mohler et al., Arzneim.-Forsch. 16, 1524 (1966). Metabolic studies: Mohler et al., Arch. Pharm. 299, 448 (1966).
CAS Name: 7-[2-(Dimethylamino)ethyl]-3,7-dihydro-1,3-dimethyl-1H-purine-2,6-dione
Additional Names: 7-(2-dimethylaminoethyl)theophylline; 1,3-dimethyl-7-(2-dimethylaminoethyl)xanthine
Tradem...
Literature References: Prepn from theophylline and dimethyl-2-chloroethylamine: Moussalli et al., GB 669070 (1952), C.A. 47, 5435i (1953); Klosa, Arch. Pharm. 288, 301 (1955). Pharmacology: Balatre, Merlen, Therapie 11, 1146 (1956); Yago, Jpn. Circ. J. 26, 407 (1962).
即日起可免费注册成为会员, 建立企业产品库, 免费上传产品目录, 企业介绍等. 让你的产品直接呈现给客户.
试运营阶段,所有广告业务5折优惠
