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3-(2-甲氧基苯基)丙腈（CAS 145851-06-5）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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12 条反应 · 12 篇文献
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 according to EXAMPLE 11 from 2-amino-3-methoxybenzaldehyde and 3-(2-methoxyphenyl)propionitrile.
来源 ID: ord-1bf1d99675514c599c01d46277640128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 according to EXAMPLE 11 from 2-amino-4-fluoro-5-morpholin-4-ylbenzaldehyde and 3-(2-methoxyphenyl)propionitrile.
来源 ID: ord-03069c92e9a2403388dd730a18871537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 according to EXAMPLE 11 from 2-amino-4-fluoro-5-morpholin-4-ylbenzaldehyde and 3-(2-methoxyphenyl)propionitrile.
来源 ID: ord-03069c92e9a2403388dd730a18871537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 according to EXAMPLE 11 from 2-amino-5-morpholin-4-ylbenzaldehyde and 3-(2-methoxyphenyl)propionitrile.
来源 ID: ord-de7ee68fa8dc4fb5be480312de3b5e7e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 according to EXAMPLE 11 from 2-amino-5-(2-methoxy-ethoxy)benzaldehyde and 3-(2-methoxyphenyl)propionitrile.
来源 ID: ord-38cde8ba697a48e8a580e4f3ad75740e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 according to EXAMPLE 11 from 2-amino-4,5-difluorobenzaldehyde and 3-(2-methoxyphenyl)propionitrile.
来源 ID: ord-6598bcf8a9de4e748cb24c774fbfcc4e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 according to EXAMPLE 11 from 2-amino-4-fluorobenzaldehyde and 3-(2-methoxyphenyl)propionitrile.
来源 ID: ord-4e759a6b177043409d2b062e1a05cb9a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 according to EXAMPLE 11 from 2-amino-4,5-difluorobenzaldehyde and 3-(2-methoxyphenyl)propionitrile.
来源 ID: ord-6598bcf8a9de4e748cb24c774fbfcc4e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 according to EXAMPLE 11 from 3-amino-2-pyridine carboxaldehyde trifluoroacetate (in turn synthesized from (2-formylpyridin-3-yl)carbamate tert-butyl ester by treatment with trifluoroacetic acid) and 3-(2-methoxyphenyl)propionitrile. One equivalent of potassium tert-butylate was additionally used.
来源 ID: ord-b2236520e32e4b318970e2b86699e7a1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 according to EXAMPLE 11 from 3-amino-4-pyridine carboxaldehyde and 3-(2-methoxyphenyl)propionitrile.
来源 ID: ord-1f71be75ebc74c42a3e67ab9d14432c2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 according to EXAMPLE 11 from 4-aminonicotinaldehyde and 3-(2-methoxyphenyl)propionitrile.
来源 ID: ord-680019e762b64028bc80efcee60e4e51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 according to EXAMPLE 11 from 2-amino-5-ethoxybenzaldehyde and 3-(2-methoxyphenyl)propionitrile.
来源 ID: ord-c8d1463b0c9a408a9dc1109a27100e06PubChem References
以下资料来自该化合物的公开数据库参考记录。