
CAS Name: 4-Piperidinecarboxylic acid
Additional Names: hexahydroisonicotinic acid
Percent Composition: C 55.79%, H 8.58%, N 10.84%, O 24.77%
Literature References: Prepd by reduction of isonicotinic acid in glacial acetic acid in the presence of platinum oxide: Wibaut, Rec. Trav. Chim. 63, 141 (1944); by reduction of isonicotinic acid in H2O and concd HCl with PtO2: Sperber et al., US 2739968 (1956 to Schering); Freifelder, US 3159639 (1964 to Abbott).
CAS Name: 1-Phenyl-1,2-ethanediol
Additional Names: phenylglycol; phenylethyleneglycol; a,b-dihydroxyethylbenzene
Percent Composition: C 69.55%, H 7.30%, O 23.16%
Literature References: Prepd by reduction of phenylglyoxylic acid with LiAlH4: Nystrom, Brown, J. Am. Chem. Soc. 69, 2548 (1947); by reduction of styrene peroxide: Russel, J. Am. Chem. Soc. 75, 5011 (1953). Prepn of optically active styrene glycol: Wilhelm, Bright, Helv. Chim. Acta 37, 221 (1954).
Percent Composition: C 53.83%, H 5.16%, O 20.49%, S 20.53%
Literature References: Prepd by reduction of p-toluenesulfonyl chloride with zinc dust: Whitmore, Hamilton, Org. Synth. 2, 89 (1922). Because the sulfinic acid is difficult to dry without partial conversion to the sulfonic acid, the sodium salt, CH3C6H4SO2Na.2H2O, is usually prepd. The free sulfinic acid is then obtained as needed by dissolving the sodium salt in cold water and carefully acidifying the soln with the exact amt of HCl needed.
CAS Name: (5a)-6,7-Didehydro-4,5-epoxy-3,6-dimethoxy-17-methylmorphinan
Percent Composition: C 72.82%, H 7.40%, N 4.47%, O 15.32%
Literature References: Prepd by reduction of thebaine: Small et al., J. Am. Chem. Soc. 58, 1457 (1936); K. W. Bentley, The Chemistry of the Morphine Alkaloids (Oxford, 1954) p 204.
CAS Name: 1-Pentanamine
Additional Names: pentylamine; 1-aminopentane
Percent Composition: C 68.90%, H 15.03%, N 16.07%
Literature References: Prepd by reduction of valeronitrile with LiAlH4 and with LiAlH4-AlCl3: Nystrom, J. Am. Chem. Soc. 77, 2544 (1955).
CAS Name: 2-Aminobenzaldehyde phenylhydrazone
Percent Composition: C 73.91%, H 6.20%, N 19.89%
Literature References: Prepd by refluxing 2-nitrobenzaldehyde with phenylhydrazine: Knöpfer, Monatsh. Chem. 31, 97 (1910).
CAS Name: Carbamimidothioic acid phenylmethyl ester monohydrochloride
Percent Composition: C 47.40%, H 5.47%, Cl 17.49%, N 13.82%, S 15.82%
Literature References: Prepd by refluxing a mixture of 126 g benzyl chloride, 76 g thiourea, and 200 ml alcohol for 0.5 hr: Donleavy, J. Am. Chem. Soc. 58, 1004 (1936).
CAS Name: 1,1'-[Sulfonylbis(4,1-phenyleneimino)]bis[1-deoxy-1-sulfo-D-glucitol] disodium salt
Additional Names: p,p'-sulfonyldianiline N,N'-diglucoside disodium disulfonate; p,p'-sulfonyldianil...
Literature References: Prepd by refluxing a mixture of 4,4¢-diaminodiphenylsulfone, glucose, sodium bisulfite, and 80% ethanol: CH 234108 (1944 to B. Siegfried), C.A. 43, 4297a (1949); B. C. Jain et al., Sci. Cult. 11, 568 (1946). Structure activity study: W. Logemann, G. P. Miori, Arzneim.-Forsch. 5, 213 (1955). Clinical evaluation in ocular leprosy: A. Bouzas, Arch. Ophthalmol. 31, 629 (1971).
Additional Names: Benzoylthiocarbimide
Percent Composition: C 58.88%, H 3.09%, N 8.58%, O 9.80%, S 19.65%
Literature References: Prepd by refluxing a mixture of KSCN and benzoyl chloride in benzene at 110-120°: Ambelang, Johnson, J. Am. Chem. Soc. 61, 632 (1939). From NH3SCN, acetone and benzoyl chloride: Frank, Smith, Org. Synth. 28, 89 (1948).
CAS Name: 1,1'-Thiobisbutane
Additional Names: butylthiobutane; dibutyl sulfide
Percent Composition: C 65.68%, H 12.40%, S 21.92%
Literature References: Prepd by refluxing a soln contg sodium sulfide and sodium n-butyl sulfate for several hrs: Gray, Gutekunst, J. Am. Chem. Soc. 42, 856 (1920).
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