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 |
|---|---|---|
| Solvent-dependent enantioselective interaction of some bis-allylamide chiral selectors studied by NMR. | 2001 May 15 |
|
| 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 |
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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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SUBSTANCE RECORD
