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C1COCCC1(CN)N製品情報
4-(aminomethyl)oxan-4-amine (CAS 50289-16-2) product identity, structure identifiers and related reaction data for chemical intermediate research and sourcing review.
想定用途
専門的研究・工業用途限定
データベース ID 43608727
安全上の注意
For professional research and industrial use only. Review the supplier safety data sheet before handling.
合成データ
10 反応 · 10 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-9bb12b5d57854b9980d37d0846d9c555反応条件: temp:110.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A mixture of 4-chloro-3-nitrobenzenesulfonamide, 4-(aminomethyl)tetrahydro-2H-pyran-4-amine, hydrochloric acid and triethylamine in dioxane (10 mL) was heated at 110° C. overnight. After cooling, the mixture was diluted with water (10 mL), and filtered. After cooling filtered
ソース ID: ord-1c33dca907094ff3b418c6c1c05a23d0反応条件: temp:110.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A mixture of 4-chloro-3-nitrobenzenesulfonamide, 4-(aminomethyl)tetrahydro-2H-pyran-4-amine, hydrochloric acid and triethylamine in dioxane (10 mL) was heated at 110° C. overnight. After cooling, the mixture was diluted with water (10 mL), and filtered. After cooling filtered
ソース ID: ord-1c33dca907094ff3b418c6c1c05a23d0反応条件: temp:110.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A mixture of 4-chloro-3-nitrobenzenesulfonamide, 4-(aminomethyl)tetrahydro-2H-pyran-4-amine, hydrochloric acid and triethylamine in dioxane (10 mL) was heated at 110° C. overnight. After cooling, the mixture was diluted with water (10 mL), and filtered. After cooling filtered
ソース ID: ord-f8d23405ece94d8b8d6f5b564b708e93反応条件: temp:110.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A mixture of 4-chloro-3-nitrobenzenesulfonamide, 4-(aminomethyl)tetrahydro-2H-pyran-4-amine, hydrochloric acid and triethylamine in dioxane (10 mL) was heated at 110° C. overnight. After cooling, the mixture was diluted with water (10 mL), and filtered. After cooling filtered
ソース ID: ord-37ef2bbed1974d41ae20258cfd891311反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-9bb12b5d57854b9980d37d0846d9c555反応条件: temp:110.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A mixture of 4-chloro-3-nitrobenzenesulfonamide, 4-(aminomethyl)tetrahydro-2H-pyran-4-amine, hydrochloric acid and triethylamine in dioxane (10 mL) was heated at 110° C. overnight. After cooling, the mixture was diluted with water (10 mL), and filtered. After cooling filtered
ソース ID: ord-fae9e5363a414d048386739003badf04反応条件: temp:110.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A mixture of 4-chloro-3-nitrobenzenesulfonamide, 4-(aminomethyl)tetrahydro-2H-pyran-4-amine, hydrochloric acid and triethylamine in dioxane (10 mL) was heated at 110° C. overnight. After cooling, the mixture was diluted with water (10 mL), and filtered. After cooling filtered
ソース ID: ord-1c33dca907094ff3b418c6c1c05a23d0反応条件: temp:110.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A mixture of 4-chloro-3-nitrobenzenesulfonamide, 4-(aminomethyl)tetrahydro-2H-pyran-4-amine, hydrochloric acid and triethylamine in dioxane (10 mL) was heated at 110° C. overnight. After cooling, the mixture was diluted with water (10 mL), and filtered. After cooling filtered
ソース ID: ord-f8d23405ece94d8b8d6f5b564b708e93反応条件: temp:110.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A mixture of 4-chloro-3-nitrobenzenesulfonamide, 4-(aminomethyl)tetrahydro-2H-pyran-4-amine, hydrochloric acid and triethylamine in dioxane (10 mL) was heated at 110° C. overnight. After cooling, the mixture was diluted with water (10 mL), and filtered. After cooling filtered
ソース ID: ord-37ef2bbed1974d41ae20258cfd891311PubChem References
化合物の公開データベース記録に掲載された情報源です。