Melting point	149-152 ºC
Water Solubility	溶解 in cold water

Symbol(GHS)	Xi
Hazard Codes	R36/37/38
SDS/MSDS	S26;S37/39

Source	SDS/MSDS Samples
没有数据	没有数据

Synthetic Route

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Name	CAS

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Articles

Peer-Reviewed Papers

Thianthrene as an activating group for the synthesis of poly (aryl ether thianthrene)s by nucleophilic aromatic substitutionEdson JB and Knauss DM Journal of Polymer Science Part A: Polymer Chemistry, 42(24), 6353-6363 (2004) Intermolecular N-alkylation of amines under conditions of the Mitsunobu reaction: a new solid-phase synthesis of tertiary benzylaminesZaragoza, Florencio and Stephensen, Henrik Tetrahedron Letters, 41(11), 1841-1844 (2000) Effects of slow-release urea and rumen-protected methionine and histidine on performance of dairy cows.F Giallongo et al.Journal of dairy science, 98(5), 3292-3308 (2015-03-03) Preparation of Fluorinated Tetrahydropyrans and Piperidines using a New Nucleophilic Fluorination Reagent DMPU/HFOkoromoba OE, et al. Organic Letters, 17(16), 3975-3977 (2015) Synthesis, 1243-1243 (1993) Protecting Groups: Strategies and Applications in Carbohydrate Chemistry, 41(11), 337-370 (2019) Liebigs Ann. Chem., 683-683 (1993) Highly Enantioselective Intramolecular Cyanoamidation:(+)-Horsfiline,(-)-Coerulescine, and (-)-EsermetholeReddy VJ and Douglas CJ Organic Letters, 12(5), 952-955 (2010) Polym. Bull., 30, 25-25 (1993) Highly regioselective synthesis of 1-aryl-3, 4, 5-substituted pyrazoles.Gosselin F, et al. Synlett, 2006(19), 3267-3270 (2006)

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