Results 211 to 220 of about 41,174 (227)
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2013
[848821-55-6] C9H9N3S (MW 155.119) InChI = 1S/C9H9N3S/c1-2-4-9(5-3-1)6-13-12-8-10-7-11-12/h1-5,7-8H,6H2 InChIKey = HRFCPTKKHXWGTB-UHFFFAOYSA-N (electrophilic reagent for the asymmetric α sulfenylation of carbonyl compounds) Solubility: soluble in ether, CH2Cl2, toluene, and benzene.
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[848821-55-6] C9H9N3S (MW 155.119) InChI = 1S/C9H9N3S/c1-2-4-9(5-3-1)6-13-12-8-10-7-11-12/h1-5,7-8H,6H2 InChIKey = HRFCPTKKHXWGTB-UHFFFAOYSA-N (electrophilic reagent for the asymmetric α sulfenylation of carbonyl compounds) Solubility: soluble in ether, CH2Cl2, toluene, and benzene.
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Synthesis of 3,4,5-Trisubstituted-1,2,4-triazoles
Chemical Reviews, 2010Moulin, Aline +5 more
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Synthesis of 2,5‐Dibromo‐1,2,4‐triazole by Bromination of 1,2,4‐Triazole
Angewandte Chemie International Edition in English, 1965C.‐F. Kröger, H. Frank
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102. 1,2,4-Triazoles. Part II. 3-Alkyl-5-aryl-1,2,4-triazoles
Journal of the Chemical Society (Resumed), 1961D. R. Liljegren, K. T. Potts
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