Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C10H10 |
| Molecular Weight | 130.1864 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1C=CC2=C1C=CC=C2
InChI
InChIKey=LRTOHSLOFCWHRF-UHFFFAOYSA-N
InChI=1S/C10H10/c1-8-6-7-9-4-2-3-5-10(8)9/h2-8H,1H3
| Molecular Formula | C10H10 |
| Molecular Weight | 130.1864 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Sulindac derivatives that activate the peroxisome proliferator-activated receptor gamma but lack cyclooxygenase inhibition. | 2008 Aug 28 |
|
| Pyrolytic hydrocarbon growth from cyclopentadiene. | 2010 Dec 2 |
|
| Preparation of furan and thiophene-derived fulvene dialdehydes: synthesis and structural characterization of a 22-oxa-21-carbaporphyrin and a related palladium(II) organometallic complex. | 2010 Oct 1 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 08:42:12 GMT 2023
by
admin
on
Sat Dec 16 08:42:12 GMT 2023
|
| Record UNII |
XEL55RNS7J
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| Record Status |
Validated (UNII)
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| Record Version |
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13024
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38857
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767-59-9
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XEL55RNS7J
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admin on Sat Dec 16 08:42:12 GMT 2023 , Edited by admin on Sat Dec 16 08:42:12 GMT 2023
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