Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C6H11N.ClH |
| Molecular Weight | 133.619 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.C=CCNCC=C
InChI
InChIKey=PZNOBXVHZYGUEX-UHFFFAOYSA-N
InChI=1S/C6H11N.ClH/c1-3-5-7-6-4-2;/h3-4,7H,1-2,5-6H2;1H
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| 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 |
|
| Enantioselective iridium-catalyzed allylic amination of ammonia and convenient ammonia surrogates. | 2007 Sep 27 |
|
| (S)-3-Bromo-4-diallyl-amino-5-[(1R,2S,5R)-2-isopropyl-5-methyl-cyclo-hex-yloxy]furan-2(5H)-one. | 2010 Nov 24 |
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6147-66-6
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DTXSID50334807
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6954CKA5LK
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521977
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admin on Sat Dec 16 08:17:57 UTC 2023 , Edited by admin on Sat Dec 16 08:17:57 UTC 2023
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SUBSTANCE RECORD
