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2-甲基-4-氨基四氢吡喃（CAS 89584-06-5）的产品身份、结构标识及相关反应资料，供化学中间体检索、研发和采购评估使用。
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10 条反应 · 10 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-51f228b0a80c46d48f6585d582e4237c反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-34d00a38d3b4479b876c84f3ba2fbd7d反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The title compound was synthesized in analogy to Example 1, using 6-(3-chlorophenyl)-2-pyridinecarboxylic acid (CAN 863704-38-5) and tetrahydro-2-methyl-2H-pyran-4-amine (CAN 89584-06-5) as starting materials, MS (EI): m/e=331.1 [M+H]+.
来源 ID: ord-b18620c2e5614e3494a728748f98db60反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The title compound was synthesized in analogy to Example 1, using 6-(3-chlorophenyl)-2-pyridinecarboxylic acid (CAN 863704-38-5) and tetrahydro-2-methyl-2H-pyran-4-amine (CAN 89584-06-5) as starting materials, MS (EI): m/e=331.1 [M+H]+.
来源 ID: ord-b18620c2e5614e3494a728748f98db60反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The title compound was synthesized in analogy to Example 1, using 6-(3-chlorophenyl)-2-pyridinecarboxylic acid (CAN 863704-38-5) and tetrahydro-2-methyl-2H-pyran-4-amine (CAN 89584-06-5) as starting materials, MS (EI): m/e=331.1 [M+H]+.
来源 ID: ord-3ff4ec365276460aa8525a7aeb48a5ca反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The title compound was synthesized in analogy to Example 1, using 6-(3-chlorophenyl)-2-pyridinecarboxylic acid (CAN 863704-38-5) and tetrahydro-2-methyl-2H-pyran-4-amine (CAN 89584-06-5) as starting materials, MS (EI): m/e=331.1 [M+H]+.
来源 ID: ord-3ff4ec365276460aa8525a7aeb48a5ca反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-51f228b0a80c46d48f6585d582e4237c反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-34d00a38d3b4479b876c84f3ba2fbd7d反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The title compound was synthesized in analogy to Example 1, using 6-(3-chlorophenyl)-2-pyridinecarboxylic acid (CAN 863704-38-5) and tetrahydro-2-methyl-2H-pyran-4-amine (CAN 89584-06-5) as starting materials, MS (EI): m/e=331.1 [M+H]+.
来源 ID: ord-b18620c2e5614e3494a728748f98db60反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The title compound was synthesized in analogy to Example 1, using 6-(3-chlorophenyl)-2-pyridinecarboxylic acid (CAN 863704-38-5) and tetrahydro-2-methyl-2H-pyran-4-amine (CAN 89584-06-5) as starting materials, MS (EI): m/e=331.1 [M+H]+.
来源 ID: ord-3ff4ec365276460aa8525a7aeb48a5caPubChem References
以下资料来自该化合物的公开数据库参考记录。
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