추천 제품
vapor pressure
31 mmHg ( 37.7 °C)
Quality Level
분석
99.5%
양식
liquid
정제법
redistillation
refractive index
n20/D 1.414 (lit.)
bp
127 °C (lit.)
mp
<−50 °C (lit.)
solubility
water: soluble 4.01 g/L at 20 °C
density
0.742 g/mL at 25 °C (lit.)
작용기
amine
SMILES string
CCN(C(C)C)C(C)C
InChI
1S/C8H19N/c1-6-9(7(2)3)8(4)5/h7-8H,6H2,1-5H3
InChI key
JGFZNNIVVJXRND-UHFFFAOYSA-N
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일반 설명
N,N-diisopropylethylamine is an aliphatic sterically hindered amine.
애플리케이션
N,N-diisopropylethylamine may be used in the following processes:
- As an organic base in the synthesis of indenopyrones.
- As an activator for chiral iridium N, P ligand complexes which can be utilized in the hydrogenation of α,β-unsaturated nitriles.
- As a non-nucleophilic base for substitution reaction.
- As a starting material in the preparation of bis[1,2]dithiolo[1,4]thiazines and bis[1,2]dithiolopyrroles.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Flam. Liq. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
3 - Flammable liquids
WGK
WGK 2
Flash Point (°F)
49.1 °F
Flash Point (°C)
9.5 °C
개인 보호 장비
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
이미 열람한 고객
Selective Syntheses of Bis [1, 2] dithiolo [1, 4] thiazines and Bis [1, 2] dithiolopyrroles from Hunig's Base.
The Journal of Organic Chemistry, 63(7), 2189-2196 (1998)
Asymmetric Hydrogenation of α, β-Unsaturated Nitriles with Base-Activated Iridium N, P Ligand Complexes.
Angewandte Chemie (Weinheim an der Bergstrasse, Germany), 126(33), 8812-8815 (2014)
Sequential Michael Addition and Enamine-Promoted Inverse Electron Demanding Diels-Alder Reaction upon 3-Vinyl-1,2,4-triazine Platforms.
Organic Letters (2015)
Enantioselective N-heterocyclic carbene-catalyzed synthesis of indenopyrones.
Organic & Biomolecular Chemistry (2015)
Facile and Gram-scale Synthesis of Metal-free Catalysts: Toward Realistic Applications for Fuel Cells.
Scientific Reports, 5 (2015)
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