您当前所在的位置:首页 > 产品中心 > 产品信息
2-(三甲基硅烷)乙氧三苯甲基氯化膦_分子结构_CAS_82495-75-8)
点击图片或这里关闭

2-(三甲基硅烷)乙氧三苯甲基氯化膦

产品号 92742 公司名称 Sigma Aldrich
CAS号 82495-75-8 公司网站 http://www.sigmaaldrich.com
分子式 C24H30ClOPSi 电 话 1-800-521-8956
分子量 429.006661 传 真
纯 度 ≥97.0% (AT) 电子邮件
保 存 Chembase数据库ID: 147680

产品价格信息

请登录

产品别名

标题
2-(Trimethylsilyl)ethoxymethyl-triphenylphosphonium chloride
IUPAC标准名
triphenyl({[2-(trimethylsilyl)ethoxy]methyl})phosphanium chloride
IUPAC传统名
triphenyl({[2-(trimethylsilyl)ethoxy]methyl})phosphanium chloride
别名
SEM-三苯基氯化磷
SEM-triphenylphosphonium chloride

产品登记号

Beilstein号 4632507
CAS号 82495-75-8
PubChem SID 24889705
MDL号 MFCD00043159

产品性质

级别 purum
线性分子式 (CH3)3SiCH2CH2OCH2P(C6H5)3Cl
纯度 ≥97.0% (AT)
熔点 145-149 °C(lit.)
熔点 166-169 °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 26-36
保存温度 2-8°C
德国WGK号 3

产品详细信息

详细说明 (English)
Other Notes
For the preparation of 2-(trimethylsilyl)ethyl protected dienol ethers which may undergo intramolecular Diels-Alder reactions5; Homologation of carbonyl compounds6,7
Application
Reactant for:
• Enantioselective synthesis of (-)-sarain A using asymmetric Michael addition, cyclization, ring-closing metathesis, intramolecular Stille coupling, and late-state installation of tertiary amine-aldehyde proximity interaction1
• Preparation of aliphatic and alicyclic aldehydes by homologation of aldehydes2
• Wittig reactions3
• Preparation of optically active (1S,5R)-(+)-3-azabicyclo[3.2.2]non-6-en-2-one via enantioselective intramolecular cyclopropanation4
详细说明 (简体中文)
Other Notes
用于制备 2-(三甲基硅基)乙基保护二烯醇醚,该产物可经受分子内 Diels-Alder 反应5;羰基化合物的同系化反应6,7
Application
Reactant for:
• Enantioselective synthesis of (-)-sarain A using asymmetric Michael addition, cyclization, ring-closing metathesis, intramolecular Stille coupling, and late-state installation of tertiary amine-aldehyde proximity interaction1
• Preparation of aliphatic and alicyclic aldehydes by homologation of aldehydes2
• Wittig reactions3
• Preparation of optically active (1S,5R)-(+)-3-azabicyclo[3.2.2]non-6-en-2-one via enantioselective intramolecular cyclopropanation4

参考文献