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(R)-α,α-双[3,5-双(三氟甲基)苯基]-2-吡咯烷甲醇三甲基硅基醚_分子结构_CAS_908303-26-4)
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(R)-α,α-双[3,5-双(三氟甲基)苯基]-2-吡咯烷甲醇三甲基硅基醚

产品号 677213 公司名称 Sigma Aldrich
CAS号 908303-26-4 公司网站 http://www.sigmaaldrich.com
分子式 C24H23F12NOSi 电 话 1-800-521-8956
分子量 597.5118584 传 真
纯 度 电子邮件
保 存 Chembase数据库ID: 140920

产品价格信息

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产品别名

标题
(R)-α,α-Bis[3,5-bis(trifluoromethyl)phenyl]-2-pyrrolidinemethanol trimethylsilyl ether
IUPAC标准名
(2R)-2-{bis[3,5-bis(trifluoromethyl)phenyl][(trimethylsilyl)oxy]methyl}pyrrolidine
IUPAC传统名
(2R)-2-{bis[3,5-bis(trifluoromethyl)phenyl][(trimethylsilyl)oxy]methyl}pyrrolidine
别名
(R)-2-[(Bis(3,5-bis(trifluoromethyl)phenyl)]trimethylsilanyloxy)methyl]pyrrolidine
(R)-2-[(Bis(3,5-bis(trifluoromethyl)phenyl)]trimethylsilyloxy)methyl]pyrrolidine
(R)-2-[(双(3,5-双(三氟甲基)苯基)]三甲基硅烷氧基)甲基]吡咯烷
(R)-α,α-Bis[3,5-bis(trifluoromethyl)phenyl]prolinol trimethylsilyl ether
(R)-α,α-双[3,5-双(三氟甲基)苯基]脯氨醇三甲基硅醚
(R)-2-[(双(3,5-双(三氟甲基)苯基)]三甲基甲硅氧基)甲基]吡咯烷

产品登记号

PubChem SID 24885357
MDL号 MFCD09750448
CAS号 908303-26-4

产品性质

Empirical Formula (Hill Notation) C24H23F12NOSi
级别 technical grade
光学纯度 enantiomeric excess: ≥99.0% (HPLC)
闪点 >110 °C
闪点 >230 °F
熔点 46-55 °C
GHS危险品标识 GHS07
GHS警示词 Warning
GHS危险声明 H315-H319-H335
欧盟危险性物质标志 刺激性(Irritant) 刺激性(Irritant) (Xi)
MSDS下载 下载链接
个人保护装置 dust mask type N95 (US), Eyeshields, Gloves
GHS警示性声明 P261-P305 + P351 + P338
危险公开号 36/37/38
安全公开号 26
德国WGK号 3

产品详细信息

详细说明 (简体中文)
包装
1, 5 g in glass bottle
Application
Catalyst involved in:
• Cyclocondensation of enals with methylenepyrrolidines1
• Organocatalytic additions of β-ketosulfoxides to conjugated aldehydes2
• Organocatalytic aza-Michael reactions3,4
• Stereoselective propargylic alkylation of propargylic esters with aldehydes5
• Epoxidation or aziridination of α,β-unsaturated aldehydes and Feist-Benary reactions of 1,3-dicarbonyls6
Protocols & Applications
Asymmetric a-Functionalization of Aldehydes using J??rgensen's Organocatalysts
详细说明 (English)
Packaging
1, 5 g in glass bottle
Application
Catalyst involved in:
• Cyclocondensation of enals with methylenepyrrolidines1
• Organocatalytic additions of β-ketosulfoxides to conjugated aldehydes2
• Organocatalytic aza-Michael reactions3,4
• Stereoselective propargylic alkylation of propargylic esters with aldehydes5
• Epoxidation or aziridination of α,β-unsaturated aldehydes and Feist-Benary reactions of 1,3-dicarbonyls6
Protocols & Applications
Asymmetric a-Functionalization of Aldehydes using J?rgensen's Organocatalysts

参考文献