Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C6H10 |
| Molecular Weight | 82.1436 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C\C=C\CC=C
InChI
InChIKey=PRBHEGAFLDMLAL-GQCTYLIASA-N
InChI=1S/C6H10/c1-3-5-6-4-2/h3-4,6H,1,5H2,2H3/b6-4+
| Molecular Formula | C6H10 |
| Molecular Weight | 82.1436 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Facile allylic C-H bond activation on the bridging disulfide ligand in the Ru(III) dinuclear complex having a conjugated RuSSRu core. | 2001 Oct 22 |
|
| New, abridged pathway to Masamune's "southern hemisphere" intermediate for the total synthesis of bryostatin 7. | 2003 Feb 20 |
|
| A versatile hexadiene synthesis by decarboxylative sp(3)-sp(3) coupling/cope rearrangement. | 2006 Jul 24 |
|
| Ionizing radiation-induced destruction of benzene and dienes in aqueous media. | 2006 May 1 |
|
| Addition of the phenoxathiin cation radical to alkenes and nonconjugated dienes. Formation of (E)- and (Z)-(10-phenoxathiiniumyl)alkenes and (E)- and (Z)-(10-phenoxathiiniumyl)dienes on basic alumina. | 2007 Aug 3 |
|
| A pinoresinol-lariciresinol reductase homologue from the creosote bush (Larrea tridentata) catalyzes the efficient in vitro conversion of p-coumaryl/coniferyl alcohol esters into the allylphenols chavicol/eugenol, but not the propenylphenols p-anol/isoeugenol. | 2007 Sep 1 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 02:07:59 GMT 2023
by
admin
on
Sat Dec 16 02:07:59 GMT 2023
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| Record UNII |
17304456C6
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| Record Status |
Validated (UNII)
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| Record Version |
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17304456C6
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7319-00-8
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