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CCCC(CO)N製品情報
2-aminopentan-1-ol (CAS 16369-14-5) 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 249017
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
12 反応 · 12 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-97ccf715af384e11b99545ef5d9ce7b5反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-f6bd46f24d934da7866919eb4e59aa89反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-619d384ec4c04377a3bfd98f1769a8a8反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Prepared by the method of Example 231, using the product of Example 219 and 2-amino-1-pentanol. Prepared by the method of Example 231
ソース ID: ord-1561996472d14802b1f7641815bdb1ac反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 2-(1-hydroxypentan-2-yl)isoindoline-1,3-dione was prepared in a similar manner to example 9c using isobenzofuran-1,3-dione and 2-aminopentan-1-ol. Yield 62%. 1H NMR (500 MHz, CDCl3): δ 0.92 (t, 3H); 1.33 (m, 2H); 1.76 (m, 1H); 1.95 (m, 1H); 3.88 (m, 1H); 4.06 (m, 1H); 4.39 (m, 1H); 7.72 (m, 2H); 7.83 (m, 2H).
ソース ID: ord-ac942abca4034833a06754f438bd7a05反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: N-(1-hydroxypentan-2-yl)benzo[d][1,3]dioxole-5-carboxamide was prepared in a similar manner to example 4 using benzo[d][1,3]dioxole-5-carboxylic acid and 2-aminopentan-1-ol. Yield: 76%. MS (M+H, 252).
ソース ID: ord-3294ed54ce0f4bd9b23ed4931a51294d反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Prepared by the method of Example 231, using the product of Example 219 and 2-amino-1-pentanol. Prepared by the method of Example 231
ソース ID: ord-1561996472d14802b1f7641815bdb1ac反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 2-(1-hydroxypentan-2-yl)isoindoline-1,3-dione was prepared in a similar manner to example 9c using isobenzofuran-1,3-dione and 2-aminopentan-1-ol. Yield 62%. 1H NMR (500 MHz, CDCl3): δ 0.92 (t, 3H); 1.33 (m, 2H); 1.76 (m, 1H); 1.95 (m, 1H); 3.88 (m, 1H); 4.06 (m, 1H); 4.39 (m, 1H); 7.72 (m, 2H); 7.83 (m, 2H).
ソース ID: ord-ac942abca4034833a06754f438bd7a05反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 2-(1-hydroxypentan-2-yl)isoindoline-1,3-dione was prepared in a similar manner to example 9c using isobenzofuran-1,3-dione and 2-aminopentan-1-ol. Yield 62%. 1H NMR (500 MHz, CDCl3): δ 0.92 (t, 3H); 1.33 (m, 2H); 1.76 (m, 1H); 1.95 (m, 1H); 3.88 (m, 1H); 4.06 (m, 1H); 4.39 (m, 1H); 7.72 (m, 2H); 7.83 (m, 2H).
ソース ID: ord-ac942abca4034833a06754f438bd7a05反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: N-(1-hydroxypentan-2-yl)benzo[d][1,3]dioxole-5-carboxamide was prepared in a similar manner to example 4 using benzo[d][1,3]dioxole-5-carboxylic acid and 2-aminopentan-1-ol. Yield: 76%. MS (M+H, 252).
ソース ID: ord-3294ed54ce0f4bd9b23ed4931a51294d反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: N-(1-hydroxypentan-2-yl)benzo[d][1,3]dioxole-5-carboxamide was prepared in a similar manner to example 4 using benzo[d][1,3]dioxole-5-carboxylic acid and 2-aminopentan-1-ol. Yield: 76%. MS (M+H, 252).
ソース ID: ord-3294ed54ce0f4bd9b23ed4931a51294d反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-97ccf715af384e11b99545ef5d9ce7b5PubChem 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。