
CAS Name: Glycinonitrile
Additional Names: cyanomethylamine; glycine nitrile
Percent Composition: C 42.84%, H 7.19%, N 49.96%
Literature References: Prepd by the action of alcoholic HCl or H2SO4 on dimolecular or trimolecular methyleneaminoacetonitrile: Anslow, King, J. Chem. Soc. 1929, 2465.
CAS Name: Di-2-propenylcyanamide
Additional Names: N-cyanodiallylamine
Percent Composition: C 68.82%, H 8.25%, N 22.93%
Literature References: Prepd by the action of allyl bromide on disodium cyanamide: Vliet, J. Am. Chem. Soc. 46, 1307 (1924); Org. Synth. coll. vol. I, 203 (1941); North, US 1659793 (1929).
Additional Names: Magnesium diamide
Percent Composition: H 7.15%, Mg 43.13%, N 49.71%
Literature References: Prepd by the action of ammonia on an ether soln of magnesium diethyl or on magnesium activated with iodine (at 400°): Terentiew, Z. Anorg. Chem. 162, 351 (1927); Schlenk, Jr., Ber. 64, 738 (1931). Prepd from metal and liquid ammonia at high pressure: Juza, Jacobs, Angew. Chem. Int. Ed. 5, 247 (1966); eidem, Z. Anorg. Allg. Chem. 370, 245 (1969).
CAS Name: Thioantimonic acid tris(2-amino-2-oxoethyl) ester
Additional Names: mercaptoacetamide antimony derivative; antimony thioglycollic acid triamide
Percent Composition: C 18.38%, H 3.0...
Literature References: Prepd by the action of ammonia on ethyl antimony thioglycollate in absolute alc. The ethyl antimony glycollate is prepd from ethyl thioglycollate and antimony trioxide: Rowntree, Abel, J. Pharmacol. 2, 109 (1910). cf. Christiansen, Organic Derivatives of Antimony, A.C.S. Monograph Series No. 24, (New York, 1925).
CAS Name: N-(Phenylmethylene)benzenamine
Additional Names: benzalaniline
Percent Composition: C 86.16%, H 6.12%, N 7.73%
Literature References: Prepd by the action of aniline on benzaldehyde: Bigelow, Eatough, Org. Synth. coll. vol. I (2nd ed., 1941) p 80. Molecular structure: M. Traetteberg et al., J. Mol. Struct. 48, 395 (1978).
CAS Name: N-(Aminocarbonyl)benzeneacetamide
Additional Names: (phenylacetyl)urea; phenacetylurea
Trademarks: Epiclase (Bellon); Phacetur; Phenurone (Abbott); Phetylureum (Katwijk)
Percent...
Literature References: Prepd by the action of aq NH3 on phenacetylurethan: Basterfield, Greig, Can. J. Res. 8, 454 (1933); of phenacetyl chloride on urea: Spielman et al., J. Am. Chem. Soc. 70, 4189 (1948). Toxicity study: K. Nakamura et al., Arzneim.-Forsch. 18, 524 (1968).
Additional Names: Malonamide nitrile
Percent Composition: C 42.85%, H 4.80%, N 33.32%, O 19.03%
Literature References: Prepd by the action of aq or alcoholic ammonia on cyanoacetic ester: Hesse, Am. Chem. J. 18, 724 (1896); Thole, Thorpe, J. Chem. Soc. 99, 429 (1911); Ott, Löpmann, Ber. 55, 1258 (1922); Corson et al., Org. Synth. coll. vol. I (2nd ed., 1941) p 179.
CAS Name: (3-Amino-4-hydroxyphenyl)arsonous dichloride monohydrochloride
Additional Names: (3-amino-4-hydroxyphenyl)dichloroarsine hydrochlorideTrademarks: Arseclor; Chlorarsen; Chlorarsol; Clo...
Literature References: Prepd by the action of arsenic trichloride on o-aminophenol, or from the corresp arsine oxide and an excess of HCl: DE 281101; from arsphenamine by treatment with mercuric chloride and HCl gas: Binz, Bauer, Z. Angew. Chem. 34, 261 (1921). Toxicity: Beck, Proc. Soc. Exp. Biol. Med. 78, 392 (1951).
CAS Name: (2-Mercapto-N-phenylacetamidato-O,S)gold
Additional Names: [[(phenylcarbamoyl)methyl]thio]gold; a-auromercaptoacetanilide; 2-mercaptoacetanilide S-gold derivative; aurothioglycolic ac...
Literature References: Prepd by the action of aurous bromide on thioglycolic acid anilide: Lewenstein, US 2451841 (1948).
CAS Name: 4-Hydroxy-4-methyl-2-pentanone
Trademarks: Pyranton
Percent Composition: C 62.04%, H 10.41%, O 27.55%
Literature References: Prepd by the action of barium hydroxide or of calcium hydroxide on acetone: Conant, Tuttle, Org. Synth. vol. 1, p 45 (1921); coll. vol. I, 193; cf. Jacquemain, Compt. Rend. 196, 1622 (1933). Industrial process using KOH and acetone: Schmitt, Disteldorf, DE 1052970 (1959 to Hibernia). Toxicity study: Smyth, Carpenter, J. Ind. Hyg. Toxicol. 30, 63 (1948).
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