| 品牌 | 货号 | 期货/现货 | 规格 | 价格 | 数量 |
|---|---|---|---|---|---|
| 阿拉丁 | I168221-1g | 现货 | 1g | 106.9 |
|
| 阿拉丁 | I168221-5g | 现货 | 5g | 696.9 |
|
| 阿拉丁 | I168221-25g | 期货 | 25g | 1908.9 |
|
| 别名 | (S)-(-)-N-甲基-1-苯乙胺|(S)-(-)-α-甲基-N-甲基苄胺 |
|---|---|
| 英文别名 | 19131-99-8|(S)-(-)-N-Methyl-1-phenylethylamine|(S)-N-Methyl-1-phenylethanamine|(1S)-N-methyl-1-phenylethanamine|N-Methyl-1-phenylethylamine, (S)-|(S)-(-)-N,alpha-Dimethylbenzylamine|4MU17YEN7Y|(S)-N,|A-Dimethylbenzylamine|CHEMBL1907958|n-methyl-(s)-1-phen |
| 规格或纯度 | 98% |
| 英文名称 | (S)-(-)-N,α-Dimethylbenzylamine |
| 储存温度 | 室温,充氩 |
| 运输条件 | 常规运输 |
| 产品介绍 | Product Describtion: (S)-(-)-N,a-Dimethylbenzylamine may be used along with benzaldehyde in the Mannich-type aminoalkylation of 2-naphthol to form 1-((S)-phenyl(((1′S)-1′-phenylethyl)methylamino)methyl)-2-naphthol. This optically active tertiary aminonaphthol can catalyze the enantioselective alkenylation of various aldehyde to generate chiral (E)- allyl alcohols |
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