추천 제품
Quality Level
제품 라인
ReagentPlus®
분석
99%
형태
crystals
불순물
1% triethylamine hydrobromide
pH
6.5 (100 g/L)
mp
285 °C (dec.) (lit.)
SMILES string
[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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관련 카테고리
애플리케이션
- Tetraethylammonium bromide (TEAB) catalyzes the synthesis of thioesters by the oxidative coupling of aldehydes or alcohols with thiols or disulfides.
- It is used as a catalyst, along with o-iodoxybenzoic acid (IBX), in the oxidation of sulfides to sulfoxides and primary carboxamides to one-carbon dehomologated nitriles.
- TEAB can also be used as an organic template to synthesize zeolite beta.
법적 정보
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
유해 및 위험 성명서
예방조치 성명서
Hazard Classifications
Aquatic Chronic 3
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
361.4 °F - closed cup
Flash Point (°C)
183 °C - closed cup
개인 보호 장비
dust mask type N95 (US), Eyeshields, Gloves
이미 열람한 고객
Tetraethylammonium Bromide-Catalyzed Oxidative Thioesterification of Aldehydes and Alcohols.
advanced synthesis and catalysis, 355(18), 3558-3562 (2013)
A mild, chemoselective oxidation of sulfides to sulfoxides using o-iodoxybenzoic acid and tetraethylammonium bromide as catalyst.
The Journal of Organic Chemistry, 68(13), 5422-5425 (2003)
Strategies for Enhancing the Catalytic Performance of Metal-Organic Frameworks in the Fixation of CO
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
Hydrothermal crystallization of zeolite beta using tetraethylammonium bromide.
Zeolites, 14(4), 295-302 (1994)
o-Iodoxybenzoic acid-and tetraethylammonium bromide-mediated oxidative transformation of primary carboxamides to one-carbon dehomologated nitriles.
The Journal of Organic Chemistry, 72(2), 662-665 (2007)
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