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- Sulfinyl_halide abstract "Sulfinyl halide groups occur when a sulfinyl functional group is singly bonded to a halogen atom. They have the general formula R-S(O)-X, where X is a halogen, and are intermediate in oxidation level between sulfenyl halides, R-S-X, and sulfonyl halides, R-SO2-X. The best known examples are sulfinyl chlorides, thermolabile, moisture-sensitive compounds, which are useful intermediates for preparation of other sufinyl derivatives such as sulfinamides, sulfinates, sulfoxides and thiosulfinates. Unlike the sulfur atom in sulfonyl halides and sulfenyl halides, the sulfur atom in sulfinyl halides is chiral, as shown for methanesulfinyl chloride.".
- Sulfinyl_halide thumbnail Methanesulfinyl_chloride.svg?width=300.
- Sulfinyl_halide wikiPageID "35600546".
- Sulfinyl_halide wikiPageLength "5147".
- Sulfinyl_halide wikiPageOutDegree "25".
- Sulfinyl_halide wikiPageRevisionID "660428822".
- Sulfinyl_halide wikiPageWikiLink Acetic_anhydride.
- Sulfinyl_halide wikiPageWikiLink Category:Halides.
- Sulfinyl_halide wikiPageWikiLink Category:Organosulfur_compounds.
- Sulfinyl_halide wikiPageWikiLink Chiral.
- Sulfinyl_halide wikiPageWikiLink Chirality.
- Sulfinyl_halide wikiPageWikiLink Dimethyl_disulfide.
- Sulfinyl_halide wikiPageWikiLink Dynamic_kinetic_resolution.
- Sulfinyl_halide wikiPageWikiLink Friedel–Crafts.
- Sulfinyl_halide wikiPageWikiLink Friedel–Crafts_reaction.
- Sulfinyl_halide wikiPageWikiLink Glucose.
- Sulfinyl_halide wikiPageWikiLink Grignard_reaction.
- Sulfinyl_halide wikiPageWikiLink Halogen.
- Sulfinyl_halide wikiPageWikiLink Kinetic_resolution.
- Sulfinyl_halide wikiPageWikiLink Lachrymatory_agent.
- Sulfinyl_halide wikiPageWikiLink Onion.
- Sulfinyl_halide wikiPageWikiLink Sulfenyl_chloride.
- Sulfinyl_halide wikiPageWikiLink Sulfenyl_halide.
- Sulfinyl_halide wikiPageWikiLink Sulfinamide.
- Sulfinyl_halide wikiPageWikiLink Sulfinic_acid.
- Sulfinyl_halide wikiPageWikiLink Sulfinyl.
- Sulfinyl_halide wikiPageWikiLink Sulfonyl_halide.
- Sulfinyl_halide wikiPageWikiLink Sulfoxide.
- Sulfinyl_halide wikiPageWikiLink Syn-Propanethial-S-oxide.
- Sulfinyl_halide wikiPageWikiLink Syn-propanethial-S-oxide.
- Sulfinyl_halide wikiPageWikiLink Tear_gas.
- Sulfinyl_halide wikiPageWikiLink Thiosulfinate.
- Sulfinyl_halide wikiPageWikiLink Triethylamine.
- Sulfinyl_halide wikiPageWikiLink File:Methanesulfinyl_chloride.svg.
- Sulfinyl_halide wikiPageWikiLinkText "Sulfinyl halide".
- Sulfinyl_halide wikiPageWikiLinkText "sulfinyl halide".
- Sulfinyl_halide wikiPageWikiLinkText "sulfinyl halide#Sulfinyl chlorides".
- Sulfinyl_halide hasPhotoCollection Sulfinyl_halide.
- Sulfinyl_halide wikiPageUsesTemplate Template:Reflist.
- Sulfinyl_halide subject Category:Halides.
- Sulfinyl_halide subject Category:Organosulfur_compounds.
- Sulfinyl_halide comment "Sulfinyl halide groups occur when a sulfinyl functional group is singly bonded to a halogen atom. They have the general formula R-S(O)-X, where X is a halogen, and are intermediate in oxidation level between sulfenyl halides, R-S-X, and sulfonyl halides, R-SO2-X. The best known examples are sulfinyl chlorides, thermolabile, moisture-sensitive compounds, which are useful intermediates for preparation of other sufinyl derivatives such as sulfinamides, sulfinates, sulfoxides and thiosulfinates.".
- Sulfinyl_halide label "Sulfinyl halide".
- Sulfinyl_halide sameAs Sulfinsäurehalogenide.
- Sulfinyl_halide sameAs m.0jkx9gh.
- Sulfinyl_halide sameAs Q425024.
- Sulfinyl_halide sameAs Q425024.
- Sulfinyl_halide sameAs 亚磺酰卤.
- Sulfinyl_halide wasDerivedFrom Sulfinyl_halide?oldid=660428822.
- Sulfinyl_halide depiction Methanesulfinyl_chloride.svg.
- Sulfinyl_halide isPrimaryTopicOf Sulfinyl_halide.