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
C=CC1=CC(C=C)=CC=C1
InChI
InChIKey=PRJNEUBECVAVAG-UHFFFAOYSA-N
InChI=1S/C10H10/c1-3-9-6-5-7-10(4-2)8-9/h3-8H,1-2H2
| 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 |
|---|---|---|
| Rhodium-catalyzed mono- and divinylation of 1-phenylpyrazoles and related compounds via regioselective C-H bond cleavage. | 2009-09-18 |
|
| Determination of ochratoxin A in human urine by solid-phase microextraction coupled with liquid chromatography-fluorescence detection. | 2007-08-15 |
|
| Flexing the muscles of m-divinylbenzene: direct measurement of the barriers to conformational isomerization. | 2007-05-17 |
|
| Isomer-specific ultraviolet spectroscopy of m- and p-divinylbenzene. | 2007-05-17 |
|
| Bridge dominated oxidation of a diruthenium 1,3-divinylphenylene complex. | 2004-09-07 |
|
| Preparation of monodisperse porous polymethacrylate microspheres and their application in the capillary electrochromatography of macrolide antibiotics. | 2002-03-01 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:12:34 GMT 2025
by
admin
on
Mon Mar 31 18:12:34 GMT 2025
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| Record UNII |
4S46QL2WFU
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| Record Status |
Validated (UNII)
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| Record Version |
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108-57-6
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7941
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203-595-7
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4S46QL2WFU
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admin on Mon Mar 31 18:12:34 GMT 2025 , Edited by admin on Mon Mar 31 18:12:34 GMT 2025
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PRIMARY |