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Merck
CN

241059

Sigma-Aldrich

溴化四乙铵

ReagentPlus®, 99%

别名:

TEAB, 四乙溴铵

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About This Item

线性分子式:
(C2H5)4N(Br)
CAS号:
分子量:
210.16
Beilstein:
3563430
EC 号:
MDL编号:
UNSPSC代码:
12352107
PubChem化学物质编号:
NACRES:
NA.22

质量水平

产品线

ReagentPlus®

检测方案

99%

形式

crystals

杂质

1% triethylamine hydrobromide

pH值(酸碱度)

6.5 (100 g/L)

mp

285 °C (dec.) (lit.)

SMILES字符串

[Br-].CC[N+](CC)(CC)CC

InChI

1S/C8H20N.BrH/c1-5-9(6-2,7-3)8-4;/h5-8H2,1-4H3;1H/q+1;/p-1

InChI key

HWCKGOZZJDHMNC-UHFFFAOYSA-M

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应用

  • 四乙基溴化铵(TEAB)可以催化醛或醇与硫醇或二硫化物的氧化偶联反应,合成硫酯。
  • 它与碘酰基苯甲酸(IBX)一起用作催化剂,将硫化物氧化成亚砜并将伯酰胺氧化成单碳dehomologated腈。
  • TEAB也可用作合成沸石β的有机模板。

法律信息

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

危险声明

预防措施声明

危险分类

Aquatic Chronic 3

WGK

WGK 3

闪点(°F)

closed cup

闪点(°C)

closed cup

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves


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Tetraethylammonium Bromide-Catalyzed Oxidative Thioesterification of Aldehydes and Alcohols.
Zhu, Xuebin et al.
advanced synthesis and catalysis, 355(18), 3558-3562 (2013)
Hydrothermal crystallization of zeolite beta using tetraethylammonium bromide.
Eapen M
Zeolites, 14(4), 295-302 (1994)
A mild, chemoselective oxidation of sulfides to sulfoxides using o-iodoxybenzoic acid and tetraethylammonium bromide as catalyst.
Shukla V
The Journal of Organic Chemistry, 68(13), 5422-5425 (2003)
o-Iodoxybenzoic acid-and tetraethylammonium bromide-mediated oxidative transformation of primary carboxamides to one-carbon dehomologated nitriles.
Bhalerao D
The Journal of Organic Chemistry, 72(2), 662-665 (2007)
Masoumeh Taherimehr et al.
ChemSusChem, 10(6), 1283-1291 (2016-12-20)
Metal-organic frameworks (MOFs) with accessible Lewis acid sites are finding increasing application in the field of heterogeneous catalysis. However, the structural instability of MOFs when they are exposed to high temperature and/or high pressure often limits their applicability. In this

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