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2,8,9-三异丙基-2,5,8,9-四硫唑嘌呤-1-磷杂双环[3,3,3]十一烷_分子结构_CAS_175845-21-3)
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2,8,9-三异丙基-2,5,8,9-四硫唑嘌呤-1-磷杂双环[3,3,3]十一烷

产品号 556955 公司名称 Sigma Aldrich
CAS号 175845-21-3 公司网站 http://www.sigmaaldrich.com
分子式 C15H33N4P 电 话 1-800-521-8956
分子量 300.423081 传 真
纯 度 电子邮件
保 存 Chembase数据库ID: 142369

产品价格信息

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产品别名

标题
2,8,9-Triisopropyl-2,5,8,9-tetraaza-1-phosphabicyclo[3,3,3]undecane
IUPAC标准名
2,8,9-tris(propan-2-yl)-2,5,8,9-tetraaza-1-phosphabicyclo[3.3.3]undecane
IUPAC传统名
2,8,9-triisopropyl-2,5,8,9-tetraaza-1-phosphabicyclo[3.3.3]undecane
别名
[2,5,8,9-Tetraaza-1-phosphabicyclo[3.3.3]undecane-2,8,9-tris(1-methylethyl)]
[2,5,8,9-四氮杂-1-磷杂双环[3.3.3]十一烷-2,8,9-三(1-甲基乙基)]

产品登记号

MDL号 MFCD03701530
PubChem SID 24879596
CAS号 175845-21-3

产品性质

线性分子式 PN(CH(CH3)2)CH2CH2NCH2CH2N(CH(CH3)2)(CH2CH2N(CH(CH3)2))
密度 0.922 g/mL at 25 °C(lit.)
闪点 85 °C
闪点 185 °F
折射率 n20/D 1.4830(lit.)
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个人保护装置 Eyeshields, Gloves, half-mask respirator (US), multi-purpose combination respirator cartridge (US)
德国WGK号 3

产品详细信息

详细说明 (English)
Application
Catalyst used in the synthesis of β-hydroxyesters and α,β-unsaturated esters8
Base used in an attempt to produce higherly reactive no-carrier-added fluoride for labeling of radiopharmaceuticals1 and used in the synthesis of monomeric alumatranes2Deprotonation agent used to study the nucleophilic reactivities of benzenesulfonyl-substituted carbanions3Catalyst involved in:
• Synthesis of polymer-supported proazaphosphatranes for catalysis of amidation and transesterification reactions4
• Wadsworth-Emmons reactions5
• Mukaiyama aldol reactions6
• Synthesis of aryl alcohols via addition reactions7
Packaging
1, 5 g in glass bottle
详细说明 (简体中文)
Application
作为催化剂用于 β-羟基酯和 α,β-不饱和酯的合成8
Base used in an attempt to produce higherly reactive no-carrier-added fluoride for labeling of radiopharmaceuticals1 and used in the synthesis of monomeric alumatranes2Deprotonation agent used to study the nucleophilic reactivities of benzenesulfonyl-substituted carbanions3Catalyst involved in:
• Synthesis of polymer-supported proazaphosphatranes for catalysis of amidation and transesterification reactions4
• Wadsworth-Emmons reactions5
• Mukaiyama aldol reactions6
• Synthesis of aryl alcohols via addition reactions7
包装
1, 5 g in glass bottle

参考文献