Name: Name:2-Propen-1-amine, N-2-propen-1-yl-
Brand: Angene
SKU: AG000LD1
Rating: 90 (10 reviews)

Catalog Number:

AG000LD1

Chemical Name:

2-Propen-1-amine, N-2-propen-1-yl-

CAS Number:

124-02-7

Molecular Formula:

C6H11N

Molecular Weight:

97.1582

MDL Number:

MFCD00008642

IUPAC Name:

N-prop-2-enylprop-2-en-1-amine

InChI:

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

InChI Key:

DYUWTXWIYMHBQS-UHFFFAOYSA-N

SMILES:

C=CCNCC=C

EC Number:

204-671-2

UNII:

N18EXB6V6P

NSC Number:

20948

RTECS Number:

UC6650000

UN Number:

2359

Complexity:

49.2

Compound Is Canonicalized:

Yes

Covalently-Bonded Unit Count:

Defined Atom Stereocenter Count:

Defined Bond Stereocenter Count:

Exact Mass:

97.089g/mol

Formal Charge:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

Isotope Atom Count:

Molecular Weight:

97.161g/mol

Monoisotopic Mass:

97.089g/mol

Rotatable Bond Count:

Topological Polar Surface Area:

12A^2

Undefined Atom Stereocenter Count:

Undefined Bond Stereocenter Count:

XLogP3:

1.1

Title	Journal
Tandem reactions of 1,2,4-oxadiazoles with allylamines.	Organic letters 20110902
(5S)-3-Chloro-4-diallyl-amino-5-[(1R,2S,5R)-2-isopropyl-5-methyl-cyclo-hex-yloxy]furan-2(5H)-one.	Acta crystallographica. Section E, Structure reports online 20110801
Synthesis and antibacterial activity of pentacyclines: a novel class of tetracycline analogs.	Journal of medicinal chemistry 20110609
(S)-3-Bromo-4-diallyl-amino-5-[(1R,2S,5R)-2-isopropyl-5-methyl-cyclo-hex-yloxy]furan-2(5H)-one.	Acta crystallographica. Section E, Structure reports online 20101201
Secondary and tertiary polydiallylammonium salts: novel polymers with high antimicrobial activity.	Biomacromolecules 20091109
Enantioselective iridium-catalyzed allylic amination of ammonia and convenient ammonia surrogates.	Organic letters 20070927
Phosphonyl, phosphonothioyl, phosphonodithioyl, and phosphonotrithioyl radicals: generation and study of their addition onto alkenes.	The Journal of organic chemistry 20031226
Novel UV cured coatings and adhesives based on the photoinitiated cyclopolymerization of derivatives of diallylamine.	Chemical communications (Cambridge, England) 20031021
A theoretical study on the mechanism of the cyclopolymerization of diallyl monomers.	The Journal of organic chemistry 20030808
Evaluation of a chiral stationary phase derived from a simple Diels-Alder reaction.	Chirality 20030515
Theoretical study of factors controlling rates of cyclization of radical intermediates from diallylamine and diallylammonium monomers in radical polymerizations.	The Journal of organic chemistry 20020726
Quantitative structure-activity relationships for a series of symmetrical bisquaternary anticancer compounds.	Bioorganic & medicinal chemistry 20020701
Cyclization of electron-deficient cyclopentadienone with 2-alkenyl and 2-alkynylamines via sequential pericyclic reaction pathway.	The Journal of organic chemistry 20011228
Solvent-dependent enantioselective interaction of some bis-allylamide chiral selectors studied by NMR.	Chirality 20010515