N,N-Diisopropylethylamine - Wikipedia
N,N-Diisopropylethylamine, or Hünig's base, is an organic compound that is a tertiary amine. It is named after the German chemist Siegfried Hünig [ de ]. It is used in organic chemistry as a non-nucleophilic base. It is commonly abbreviated as DIPEA,DIEA, or i-Pr2NEt.
N,N-Diisopropylethylamine - Wikiwand
Structure. DIPEA consists of a central nitrogen atom that is bonded to an ethyl group and two isopropyl groups. A lone pair of electrons resides on the nitrogen atom, which can react with electrophiles.
diisopropylethylamine | C8H19N - ChemSpider
ChemSpider record containing structure, synonyms, properties, vendors and database links for diisopropylethylamine, 7087-68-5, DIEA.
N,N-Diisopropylethylamine ReagentPlus , = 99 7087-68-5
N,N -Diisopropylethylamine, also known as Hünig′s base, is a sterically hindered amine. It is a non-nucleophilic base commonly employed for substitution reactions. [1] It acts as an activator for chiral iridium N, P ligand complexes, which can be utilized in the hydrogenation of α, β-unsaturated nitriles. [2]
N,N-Diisopropylethylamine | C8H19N | CID 81531 - PubChem
N,N-Diisopropylethylamine | C8H19N | CID 81531 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.
Diisopropylethylamine - NIST Chemistry WebBook
Diisopropylethylamine. Formula: C 8 H 19 N. Molecular weight: 129.2432. IUPAC Standard InChI:InChI=1S/C8H19N/c1-6-9 (7 (2)3)8 (4)5/h7-8H,6H2,1-5H3 Copy. IUPAC Standard InChIKey:JGFZNNIVVJXRND-UHFFFAOYSA-N Copy. CAS Registry Number: 7087-68-5.
N,N-Diisopropylethylamine - chemeurope.com
N,N-Diisopropylethylamine, or Hünig's base, DIPEA or DIEA, is an organic compound and an amine. It is used in organic chemistry as a base. Because the nitrogen atom is shielded by the two isopropyl groups and an ethyl group only a proton is small enough to easily fit.
N-Ethyldiisopropylamine BASF quality, = 98.0 7087-68-5
It is a non-nucleophilic base commonly employed in substitution reactions, alkylations, and amide couplings, etc. DIPEA is also used as a base in the Pd catalyzed cross-coupling reactions, which include Heck coupling and Sonagashira coupling reactions.
N,N-Diisopropylethylamine (DIEA) - Common Organic Chemistry
Structure: CAS Number: 7087-68-5. Molecular Weight: 129.24 g/mol. Appearance: Colorless liquid. Boiling Point: 127 C. Density: 0.742 g/mL. DIEA is a base that is widely used in organic synthesis. The three relatively bulky alkyl groups attached to the nitrogen make DIEA a non-nucleophilic base.
N,N-Diisopropylethylamine - N-Ethyldiisopropylamine, DIPEA
N. -Diisopropylethylamine. Synonym (s): N-Ethyldiisopropylamine, DIPEA, Ethyldiisopropylamine, ‘Hünig’s base’. Linear Formula: [ (CH3)2CH]2NC2H5. CAS Number: 7087-68-5. Molecular Weight:
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