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Details

Stereochemistry ACHIRAL
Molecular Formula C8H19N
Molecular Weight 129.2432
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Diisopropylethylamine

SMILES

CCN(C(C)C)C(C)C

InChI

InChIKey=JGFZNNIVVJXRND-UHFFFAOYSA-N
InChI=1S/C8H19N/c1-6-9(7(2)3)8(4)5/h7-8H,6H2,1-5H3

HIDE SMILES / InChI

Molecular Formula C8H19N
Molecular Weight 129.2432
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Sterically hindered C(alpha, alpha)-disubstituted alpha-amino acids: synthesis from alpha-nitroacetate and incorporation into peptides.
2001 Oct 19
Practical protocols for stepwise solid-phase synthesis of cysteine-containing peptides.
2002 Nov
Use of phenyl 2-alpha-selenoglycosides of N-acetylneuraminic acid as a glycosyl donor for the glycosylation reactions.
2002 Sep 2
Peptide-bond modification for metal coordination: peptides containing two hydroxamate groups.
2003
Solid-phase synthesis and spectral properties of 2-alkylthio-6H-pyrano[2,3-f]benzimidazole-6-ones: a combinatorial approach for 2-alkylthioimidazocoumarins.
2004 Jul-Aug
Detection of bacteria with carbohydrate-functionalized fluorescent polymers.
2004 Oct 20
Synthesis and characterization of human alpha-defensins 4-6.
2004 Sep
Synthesis and photochemical properties of photoactivated antitumor prodrugs releasing 5-fluorouracil.
2005 Feb 21
Affinity enhancement bivalent morpholino for pretargeting: initial evidence by surface plasmon resonance.
2005 Mar-Apr
Inhibition of HIV derived lentiviral production by TAR RNA binding domain of TAT protein.
2005 Nov 17
Surfaces for immobilization of N-terminal cysteine derivatives via native chemical ligation.
2008 Dec 16
Selenium derivatization of nucleic acids for phase and structure determination in nucleic acid X-ray crystallography.
2008 Mar
A catalytic, Brønsted base strategy for intermolecular allylic C-H amination.
2009 Aug 26
Chemical tools selectively target components of the PKA system.
2009 Feb 12
Synthesis and spectral properties of novel fluorescent poly(oxyethylene phosphate) tris(beta-diketonate) europium (III) complexes.
2009 Jan
A second-generation ionic liquid matrix-assisted laser desorption/ionization matrix for effective mass spectrometric analysis of biodegradable polymers.
2009 Nov
Synergistic antibacterial and anti-inflammatory activity of temporin A and modified temporin B in vivo.
2009 Sep 28
tert-Butyl N-[6-(N,N-dipropyl-carbamo-yl)-1,3-benzothia-zol-2-yl]carbamate.
2010 Apr 30
4-Methyl-N-[(S)-1-phenyl-eth-yl]benzene-sulfonamide.
2010 Aug 21
Formation of a leuco spirolactone from 4-(2-carboxyphenyl)-7-diethylamino-4'-dimethylamino-1-benzopyrylium: design of a phase-change thermochromic system based on a flavylium dye.
2010 Jul 12
Stimuli of sensory-motor nerves terminate arterial contractile effects of endothelin-1 by CGRP and dissociation of ET-1/ET(A)-receptor complexes.
2010 Jun 1
Optimization of solvent bar microextraction combined with gas chromatography for the analysis of aliphatic amines in water samples.
2010 Jun 15
Extension of the PNA world by functionalized PNA monomers eligible candidates for inverse Diels Alder Click Chemistry.
2010 Jun 27
N-octanoyl dopamine, a non-hemodyanic dopamine derivative, for cell protection during hypothermic organ preservation.
2010 Mar 16
Dansylation of unactivated alcohols for improved mass spectral sensitivity and application to analysis of cytochrome P450 oxidation products in tissue extracts.
2010 Sep 15
HIV-1 gp41 and TCRalpha trans-membrane domains share a motif exploited by the HIV virus to modulate T-cell proliferation.
2010 Sep 2
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 02:27:35 GMT 2023
Edited
by admin
on Sat Dec 16 02:27:35 GMT 2023
Record UNII
5SIQ15721L
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
Diisopropylethylamine
Systematic Name English
N-Ethyl-N-(1-methylethyl)-2-propanamine
Systematic Name English
iPr2NEt
Common Name English
DIEA
Common Name English
N,N-Diisopropylethylamine
Systematic Name English
N-Ethyldiisopropylamine
Systematic Name English
Huenig's base
Common Name English
DIPEA
Common Name English
NSC-147491
Code English
Diisopropylethylamine [MI]
Common Name English
Ethyldiisopropylamine
Systematic Name English
1,1'-Dimethyltriethylamine
Common Name English
Code System Code Type Description
NSC
147491
Created by admin on Sat Dec 16 02:27:35 GMT 2023 , Edited by admin on Sat Dec 16 02:27:35 GMT 2023
PRIMARY
MERCK INDEX
m4489
Created by admin on Sat Dec 16 02:27:35 GMT 2023 , Edited by admin on Sat Dec 16 02:27:35 GMT 2023
PRIMARY Merck Index
FDA UNII
5SIQ15721L
Created by admin on Sat Dec 16 02:27:35 GMT 2023 , Edited by admin on Sat Dec 16 02:27:35 GMT 2023
PRIMARY
EPA CompTox
DTXSID8064561
Created by admin on Sat Dec 16 02:27:35 GMT 2023 , Edited by admin on Sat Dec 16 02:27:35 GMT 2023
PRIMARY
CAS
7087-68-5
Created by admin on Sat Dec 16 02:27:35 GMT 2023 , Edited by admin on Sat Dec 16 02:27:35 GMT 2023
PRIMARY
ECHA (EC/EINECS)
230-392-0
Created by admin on Sat Dec 16 02:27:35 GMT 2023 , Edited by admin on Sat Dec 16 02:27:35 GMT 2023
PRIMARY
WIKIPEDIA
N,N-DIISOPROPYLETHYLAMINE
Created by admin on Sat Dec 16 02:27:35 GMT 2023 , Edited by admin on Sat Dec 16 02:27:35 GMT 2023
PRIMARY
PUBCHEM
81531
Created by admin on Sat Dec 16 02:27:35 GMT 2023 , Edited by admin on Sat Dec 16 02:27:35 GMT 2023
PRIMARY