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N-Boc-吡咯，5176-27-2，98%
| 品牌 | 厂商性质 | 产地 | 货期 |
|---|---|---|---|
| 阿拉丁 | 总代理 | 中国 | 现货 |
性能特点
It is an N-protected pyrrole. It undergoes Diels–Alder reaction with enantiomerically pure allen
| 货号 | 规格 | CAS号 | 价格 | 操作 |
|---|---|---|---|---|
| I133868-100ml | 100ml | 5176-27-2 | ￥1,105.90 | 询底价 |
| I133868-25ml | 25ml | 5176-27-2 | ￥293.90 | 询底价 |
| I133868-5ml | 5ml | 5176-27-2 | ￥70.90 | 询底价 |
| I133868-500ml | 500ml | 5176-27-2 | ￥3,398.90 | 询底价 |
中文名：N-Boc-吡咯
英文名：N-Boc-pyrrole
中文别名：1-吡咯甲酸叔丁酯
英文别名：5176-27-2|N-Boc-pyrrole|tert-butyl 1H-pyrrole-1-carboxylate|tert-butyl pyrrole-1-carboxylate|N-T-BOC-PYRROLE|T-BUTYL 1H-PYRROLE-1-CARBOXYLATE|tert-Butyl 1-pyrrolecarboxylate|N-tert-Butoxycarbonyl-1H-pyrrole|MFCD00209559|1H-pyrrole-1-carboxylic acid, 1,1-d
纯度：98%
货号：I133868
Cas号：5176-27-2
产品介绍：
It is an N-protected pyrrole. It undergoes Diels–Alder reaction with enantiomerically pure allene-1,3-dicarboxylates to form endo-adducts with retention in configurations at two newly generated stereogenic centers.It also undergoes cyclopropanation with methyl phenyldiazoacetate to form both monocyclopropane and dicyclopropane.Its Ir-catalyzed C-H borylation followed by cross coupling with 3-chlorothiophene to form biheterocycle has been reported.A useful pyrrole building block.
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