Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C10H14 |
| Molecular Weight | 134.2182 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=CC(C)=C(C)C(C)=C1
InChI
InChIKey=BFIMMTCNYPIMRN-UHFFFAOYSA-N
InChI=1S/C10H14/c1-7-5-8(2)10(4)9(3)6-7/h5-6H,1-4H3
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Dichlorido[1-(2-methyl-benz-yl)-3-(η-2,4,6-trimethyl-benz-yl)-1H-2,3-dihydro-benzimidazol-2-yl-idene]ruthenium(II) dichloro-methane solvate. | 2009-02-04 |
|
| Solvent and spectral effects in the ultrafast charge recombination dynamics of excited donor-acceptor complexes. | 2008-01-31 |
|
| Role of intermolecular coupling in the photophysics of disordered organic semiconductors: aggregate emission in regioregular polythiophene. | 2007-05-18 |
|
| Physiologically-based toxicokinetic modeling of durene (1,2,3,5-tetramethylbenzene) and isodurene (1,2,4,5-tetramethylbenzene) in humans. | 2007 |
|
| Adsorption of single-ring organic compounds to wood charcoals prepared under different thermochemical conditions. | 2005-06-01 |
|
| Asymmetric alkylation of N-toluenesulfonylimines with dialkylzinc reagents catalyzed by copper-chiral amidophosphine. | 2003-12-12 |
|
| Eta6-mesityl,eta1-imidazolinylidene-carbene-ruthenium(II) complexes: catalytic activity of their allenylidene derivatives in alkene metathesis and cycloisomerisation reactions. | 2003-05-23 |
|
| Sonochemical preparation of supported hydrodesulfurization catalysts. | 2001-08-29 |
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
8091
Created by
admin on Mon Mar 31 18:59:37 GMT 2025 , Edited by admin on Mon Mar 31 18:59:37 GMT 2025
|
PRIMARY | |||
|
DTXSID6026119
Created by
admin on Mon Mar 31 18:59:37 GMT 2025 , Edited by admin on Mon Mar 31 18:59:37 GMT 2025
|
PRIMARY | |||
|
208-417-1
Created by
admin on Mon Mar 31 18:59:37 GMT 2025 , Edited by admin on Mon Mar 31 18:59:37 GMT 2025
|
PRIMARY | |||
|
10695
Created by
admin on Mon Mar 31 18:59:37 GMT 2025 , Edited by admin on Mon Mar 31 18:59:37 GMT 2025
|
PRIMARY | |||
|
0JBI5Y5A5Z
Created by
admin on Mon Mar 31 18:59:37 GMT 2025 , Edited by admin on Mon Mar 31 18:59:37 GMT 2025
|
PRIMARY | |||
|
Isodurene
Created by
admin on Mon Mar 31 18:59:37 GMT 2025 , Edited by admin on Mon Mar 31 18:59:37 GMT 2025
|
PRIMARY | |||
|
C021207
Created by
admin on Mon Mar 31 18:59:37 GMT 2025 , Edited by admin on Mon Mar 31 18:59:37 GMT 2025
|
PRIMARY | |||
|
m6481
Created by
admin on Mon Mar 31 18:59:37 GMT 2025 , Edited by admin on Mon Mar 31 18:59:37 GMT 2025
|
PRIMARY | Merck Index | ||
|
527-53-7
Created by
admin on Mon Mar 31 18:59:37 GMT 2025 , Edited by admin on Mon Mar 31 18:59:37 GMT 2025
|
PRIMARY |
SUBSTANCE RECORD
