추천 제품
vapor pressure
2.9 mmHg ( 50 °C)
Quality Level
제품 라인
ReagentPlus®
분석
≥99%
형태
crystals
환경친화적 대안 제품 특성
Catalysis
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refractive index
n20/D 1.4634 (lit.)
mp
156-159 °C (lit.)
density
1.02 g/mL at 25 °C (lit.)
환경친화적 대안 카테고리
, Aligned
SMILES string
N12CCN(CC2)CC1
InChI
1S/C6H12N2/c1-2-8-5-3-7(1)4-6-8/h1-6H2
InChI key
IMNIMPAHZVJRPE-UHFFFAOYSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
일반 설명
1,4-Diazabicyclo[2.2.2]octane (DABCO) is a bicyclic compound used as a strong base and catalyst in organic synthesis.
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We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for catalytic efficiency. Click here for more information.
1,4-Diazabicyclo[2.2.2]octane (DABCO, triethylenediamine), a caged tertiary diamine, is a commonly used strong hindered amine base in chemical synthesis. It can also be employed as a complexing ligand and as a catalyst. Its gas-phase electronic absorption spectrum, vibrational spectra, multiphoton ionization (MPI), and two-photon fluorescence excitation (TPFE) spectra have been recorded and analyzed. Proton magnetic resonance (PMR) studies of DABCO in solid state were conducted in order to determine its line width, second moment, and spin-lattice relaxation time.
애플리케이션
1,4-Diazabicyclo[2.2.2]octane (DABCO) may be used in the synthesis of isoxazole derivatives via dehydration of primary nitro compounds in the presence of dipolarophiles. DABCO may be used in the preparation of the following:
- DABCO bis(perhydrate)
- DABCO monohydrate
- DABCO hexahydrate
법적 정보
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Sol. 1 - Skin Irrit. 2
Storage Class Code
4.1B - Flammable solid hazardous materials
WGK
WGK 1
Flash Point (°F)
144.0 °F - closed cup
Flash Point (°C)
62.2 °C - closed cup
개인 보호 장비
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
이미 열람한 고객
Experimental vibrational spectra and computational study of 1,4-diazabicyclo [2.2.2] octane.
Journal of Molecular Structure, 1028, 134-140 (2012)
1,4-Diazabicyclo [2.2.2] octane (DABCO) as an Efficient Reagent for the Synthesis of Isoxazole Derivatives from Primary Nitro Compounds and Dipolarophiles: The Role of the Base.
European Journal of Organic Chemistry, 2006(21), 4852-4860 (2006)
Structure and Intramolecular Motions in Triethylenediamine as Studied by Gas Electron Diffraction.
Bulletin of the Chemical Society of Japan, 44(1), 72-77 (1971)
Multiphoton ionization and two-photon fluorescence excitation spectroscopy of triethylenediamine.
J. Chem. Phys., 71(3), 1241-1246 (1979)
Proton Magnetic Resonance Studies of Solid Triethylenediamine-Molecular Structure and Motions.
J. Chem. Phys., 43(12), 4325-4336 (1965)
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