U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C6H11N
Molecular Weight 97.1582
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DIALLYLAMINE

SMILES

C=CCNCC=C

InChI

InChIKey=DYUWTXWIYMHBQS-UHFFFAOYSA-N
InChI=1S/C6H11N/c1-3-5-7-6-4-2/h3-4,7H,1-2,5-6H2

HIDE SMILES / InChI

Molecular Formula C6H11N
Molecular Weight 97.1582
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Cyclization of electron-deficient cyclopentadienone with 2-alkenyl and 2-alkynylamines via sequential pericyclic reaction pathway.
2001 Dec 28
Solvent-dependent enantioselective interaction of some bis-allylamide chiral selectors studied by NMR.
2001 May 15
Quantitative structure-activity relationships for a series of symmetrical bisquaternary anticancer compounds.
2002 Jul
Theoretical study of factors controlling rates of cyclization of radical intermediates from diallylamine and diallylammonium monomers in radical polymerizations.
2002 Jul 26
A theoretical study on the mechanism of the cyclopolymerization of diallyl monomers.
2003 Aug 8
Phosphonyl, phosphonothioyl, phosphonodithioyl, and phosphonotrithioyl radicals: generation and study of their addition onto alkenes.
2003 Dec 26
Evaluation of a chiral stationary phase derived from a simple Diels-Alder reaction.
2003 May 15
Novel UV cured coatings and adhesives based on the photoinitiated cyclopolymerization of derivatives of diallylamine.
2003 Oct 21
Enantioselective iridium-catalyzed allylic amination of ammonia and convenient ammonia surrogates.
2007 Sep 27
Secondary and tertiary polydiallylammonium salts: novel polymers with high antimicrobial activity.
2009 Nov 9
(S)-3-Bromo-4-diallyl-amino-5-[(1R,2S,5R)-2-isopropyl-5-methyl-cyclo-hex-yloxy]furan-2(5H)-one.
2010 Nov 24
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:20:27 GMT 2023
Edited
by admin
on Fri Dec 15 18:20:27 GMT 2023
Record UNII
N18EXB6V6P
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DIALLYLAMINE
MI  
Systematic Name English
N-2-PROPENYL-2-PROPEN-1-AMINE [HSDB]
Common Name English
NSC-20948
Code English
DIALLYLAMINE [MI]
Common Name English
Code System Code Type Description
MERCK INDEX
m4244
Created by admin on Fri Dec 15 18:20:27 GMT 2023 , Edited by admin on Fri Dec 15 18:20:27 GMT 2023
PRIMARY Merck Index
ECHA (EC/EINECS)
204-671-2
Created by admin on Fri Dec 15 18:20:27 GMT 2023 , Edited by admin on Fri Dec 15 18:20:27 GMT 2023
PRIMARY
FDA UNII
N18EXB6V6P
Created by admin on Fri Dec 15 18:20:27 GMT 2023 , Edited by admin on Fri Dec 15 18:20:27 GMT 2023
PRIMARY
PUBCHEM
31279
Created by admin on Fri Dec 15 18:20:27 GMT 2023 , Edited by admin on Fri Dec 15 18:20:27 GMT 2023
PRIMARY
HSDB
5471
Created by admin on Fri Dec 15 18:20:27 GMT 2023 , Edited by admin on Fri Dec 15 18:20:27 GMT 2023
PRIMARY
EPA CompTox
DTXSID1024918
Created by admin on Fri Dec 15 18:20:27 GMT 2023 , Edited by admin on Fri Dec 15 18:20:27 GMT 2023
PRIMARY
CAS
124-02-7
Created by admin on Fri Dec 15 18:20:27 GMT 2023 , Edited by admin on Fri Dec 15 18:20:27 GMT 2023
PRIMARY
NSC
20948
Created by admin on Fri Dec 15 18:20:27 GMT 2023 , Edited by admin on Fri Dec 15 18:20:27 GMT 2023
PRIMARY