(1S,4S,5S)-5-(4-methoxyphenyl)-2-tosyl-2-aza-5-phosphabicyclo[2.2.1]heptane

 化学構造式
CAS番号.
化学名:
别名:
英語名:
(1S,4S,5S)-5-(4-methoxyphenyl)-2-tosyl-2-aza-5-phosphabicyclo[2.2.1]heptane
英語别名:
Exo-2-naphthyl Kwon [2.2.1] bicyclic phosphine;(1S,4S,5S)-5-(4-methoxyphenyl)-2-tosyl-2-aza-5-phosphabicyclo[2.2.1]heptane
CBNumber:
CB32897988
化学式:
C19H22NO3PS
分子量:
375.421641
MOL File:
Mol file

(1S,4S,5S)-5-(4-methoxyphenyl)-2-tosyl-2-aza-5-phosphabicyclo[2.2.1]heptane 物理性質

融点 :
153-158°C
貯蔵温度 :
2-8°C
外見 :

安全性情報

(1S,4S,5S)-5-(4-methoxyphenyl)-2-tosyl-2-aza-5-phosphabicyclo[2.2.1]heptane 価格 もっと(2)

メーカー 製品番号 製品説明 CAS番号 包装 価格 更新時間 購入
Sigma-Aldrich Japan 798347
Exo-2-Naphthyl Kwon [2.2.1] Bicyclic Phosphine
100mg ¥14500 2024-03-01 購入
Sigma-Aldrich Japan L512435
Exo-2-Naphthyl Kwon [2.2.1] Bicyclic Phosphine
50mg ¥19500 2018-12-25 購入

(1S,4S,5S)-5-(4-methoxyphenyl)-2-tosyl-2-aza-5-phosphabicyclo[2.2.1]heptane 化学特性,用途語,生産方法

使用

The bicyclic, chiral phosphine was developed by the Kwon Research Group.Its initial applications were for asymmetric [3+2] annulation between allenes and imines as well as the first examples of phosphine-catalyzed asymmetric syntheses of 1,2,3,5-substituted pyrrolines. Along with nucleophilic organocatalysis, the P-chiral phosphines may also find utility in asymmetric transition-metal catalysis.

(1S,4S,5S)-5-(4-methoxyphenyl)-2-tosyl-2-aza-5-phosphabicyclo[2.2.1]heptane 上流と下流の製品情報

原材料

準備製品


(1S,4S,5S)-5-(4-methoxyphenyl)-2-tosyl-2-aza-5-phosphabicyclo[2.2.1]heptane 生産企業

Global( 2)Suppliers
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orderCN@merckgroup.com China 51471 80

  • (1S,4S,5S)-5-(4-methoxyphenyl)-2-tosyl-2-aza-5-phosphabicyclo[2.2.1]heptane
  • Exo-2-naphthyl Kwon [2.2.1] bicyclic phosphine
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