
CAS Name: 4-Ethoxybenzenamine
Additional Names: 4-aminophenetole; 4-ethoxyaniline; p-aminophenyl ethyl ether
Percent Composition: C 70.04%, H 8.08%, N 10.21%, O 11.66%
Literature References: Prepn by reduction of p-nitrophenetole: West, J. Chem. Soc. 127, 494 (1925). Prepn from nitrobenzene, ethanol, Mg, and sulfuric acid: Yukawa, J. Chem. Soc. Jpn. 71, 547 (1950).
CAS Name: (3b,5E,7E,10a,22E)-9,10-Secoergosta-5,7,22-trien-3-ol
Additional Names: dichystrolum; anti-tetany substance 10; AT 10
Trademarks: Antitanil; Calcamine (Wander); Dygratyl (Ferrosan)...
Literature References: Prepn by reduction of tachysterol: Windaus et al., Ann. 499, 198 (1932); v. Werder, US 2228491 (1941 to Winthrop), cf. Z. Physiol. Chem. 260, 119 (1939). Activity similar to parathyroid extract.
CAS Name: 6,7-Bis(cyclopropylmethoxy)-4-hydroxy-3-quinolinecarboxylic acid ethyl ester
Additional Names: ethyl 6,7-bis(cyclopropylmethoxy)-4-hydroxyquinoline-3-carboxylate; cyproquinidate; cypr...
Literature References: Prepn by ring closure of corresp dialkyl (alkoxyphenylamino)methylenemalonates: Mizzoni et al., Experientia 24, 1188 (1968); Mizzoni, DeStevens, ZA 6705655 (1968 to Ciba), C.A. 70, 47316t (1969). Review of structure and biology: Mizzoni et al., J. Med. Chem. 13, 870 (1970).
CAS Name: 7-Amino-2-naphthalenesulfonic acid
Additional Names: 2-naphthylamine-7-sulfonic acid; b-naphthylamine-d-sulfonic acid
Percent Composition: C 53.80%, H 4.06%, N 6.27%, O 21.50%, S 1...
Literature References: Prepn by sulfonation of b-naphthylamine and separation from the 6-amino isomer: Green, J. Chem. Soc. 55, 33 (1889); from 7-hydroxy-2-naphthalenesulfonic acid and ammonia: Green, loc. cit.; Wait, US 1492497 (1924).
CAS Name: 3-Hydroxy-2-methyl-5-[(phosphonooxy)methyl]-4-pyridinecarboxaldehyde
Additional Names: pyridoxal 5-monophosphoric acid ester; 3-hydroxy-5-(hydroxymethyl)-2-methylisonicotinaldehyde 5-...
Literature References: Prepn by the action of adenosine triphosphate on pyridoxal: Gunsalus et al., J. Biol. Chem. 155, 685 (1944); by the action of phosphorus oxychloride on pyridoxal in aq soln: Gunsalus et al., ibid. 161, 743 (1945); Umbreit et al., Arch. Biochem. 7, 189 (1945); by phosphorylation of pyridoxamine with 100% H3PO4 followed by oxidation: Wilson, Harris, J. Am. Chem. Soc. 73, 4693 (1951). Alternate route: Schorre, US 3124587 (1964 to E. Merck). Isoln in pure form as the oxime and as the O-methyl oxime and structure: Heyl et al., J. Am. Chem. Soc. 73, 3430 (1951). Activity as a cotransaminase in the synthesis of amino acids: Lichstein et al., J. Biol. Chem. 161, 311 (1945). Activity of natural and synthetic material: Umbreit et al., loc. cit.
CAS Name: (T-4)-Trichlorooxovanadium
Additional Names: vanadium(V) trichloride oxide; vanadium oxytrichloride
Percent Composition: Cl 61.37%, O 9.23%, V 29.39%
Literature References: Prepn by the action of dry Cl2 on V2O3 or V2O5: Brown, Griffitts, Inorg. Synth. 1, 106 (1939); 4, 80 (1953); Oppermann, Z. Anorg. Allg. Chem. 351, 113 (1967). Toxicity data: Smyth et al., Am. Ind. Hyg. Assoc. J. 30, 470 (1969).
Additional Names: Tetrasilicon decahydride; silicobutane; tetrasilicane; tetrasilicobutane
Percent Composition: H 8.23%, Si 91.77%
Literature References: Prepn by the action of hydrochloric acid on magnesium silicide: Stock, Somiesky, Ber. 49, 111 (1916); 54B, 524 (1921); 56B, 247 (1923); Stock et al., Ber. 56, 1695 (1923); Emeleus, Maddock, J. Chem. Soc. 1946, 1131.
CAS Name: (4S)-4,5-Diamino-5-oxopentanoic acid
Additional Names: 4-amino-L-glutaramic acid; glutamic acid a-amide
Percent Composition: C 41.09%, H 6.90%, N 19.17%, O 32.84%
Literature References: Prepn by the action of NH3 on N-carbobenzyloxy-L-glutamic acid anhydride: Kozo Narita, J. Chem. Soc. Jpn. Pure Chem. Sect. 74, 832 (1953); from 1-tosylpyroglutamide by reduction with Na in NH3: Swan, du Vigneaud, J. Am. Chem. Soc. 76, 3110 (1954); from the g-methyl ester of N-tritylglutamic acid: Amiard, Heymes, US 2927118 (1960 to UCLAF).
CAS Name: 3-Phenyl-2-propenoyl chloride
Percent Composition: C 64.88%, H 4.24%, Cl 21.28%, O 9.60%
Literature References: Prepn by the action of oxalyl chloride on sodium cinnamate: Adams, Ulich, J. Am. Chem. Soc. 42, 605 (1920).
Percent Composition: C 25.01%, H 2.10%, F 39.56%, O 33.32%
Literature References: Prepn by the interaction of anhydr formic acid, potassium fluoride and benzoyl chloride (16% yield): Nyesmejanov, Kahn, Ber. 67, 203 (1946); from benzoyl fluoride and formic acid (36% yield): Masentshev, J. Gen. Chem. USSR 16, 203 (1946); from benzoyl chloride, formic acid, and KHF2 (35% yield): Olah et al., Ber. 89, 862 (1956); Olah, Kuhn, J. Am. Chem. Soc. 82, 2381 (1960); from acetic formic anhydride, CH3COOOCH, and anhydr HF (67% yield): Olah, Kuhn, ibid. 2380.
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