Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C10H10 |
| Molecular Weight | 130.1864 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C1=CC2C=CC3C1C3C=C2
InChI
InChIKey=UKFBVTJTKMSPMI-UHFFFAOYSA-N
InChI=1S/C10H10/c1-4-8-9-5-2-7(1)3-6-10(8)9/h1-10H
| Molecular Formula | C10H10 |
| Molecular Weight | 130.1864 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Aromaticity on the fly: cyclic transition state stabilization at finite temperature. | 2010-01-21 |
|
| William von Eggers Doering's many research achievements during the first 65 years of his career in chemistry. | 2009-01-20 |
|
| How important is bishomoaromatic stabilization in determining the relative barrier heights for the degenerate Cope rearrangements of semibullvalene, barbaralane, bullvalene, and dihydrobullvalene? | 2005-04-01 |
|
| Bullvalene trisepoxide and its stereospecific rearrangement to 2,8,12-trioxahexacyclo[8.3.0.0(3,9)0(4,6)0(5,13)0(7,11)]tridecane: two new C3-symmetrical oligocycles with propeller chirality. | 2005-03-18 |
|
| Thiabowls: synthesis, molecular structure, and novel supramolecular architecture of trithia-[3]-peristylane. | 2004-05-13 |
|
| Bond-shift rearrangement in solid Li(3)P(7)(monoglyme)(3): a (31)P MAS NMR study. | 2001-12 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:20:50 GMT 2025
by
admin
on
Mon Mar 31 21:20:50 GMT 2025
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| Record UNII |
ZQZ1X09E2B
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| Record Status |
Validated (UNII)
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| Record Version |
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BULLVALENE
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136796
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DTXSID80143348
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m2757
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PRIMARY | Merck Index |