Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C15H22 |
| Molecular Weight | 202.3352 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=CC=C(C=C1)[C@]2(C)CCCC2(C)C
InChI
InChIKey=SLKPBCXNFNIJSV-HNNXBMFYSA-N
InChI=1S/C15H22/c1-12-6-8-13(9-7-12)15(4)11-5-10-14(15,2)3/h6-9H,5,10-11H2,1-4H3/t15-/m0/s1
| Molecular Formula | C15H22 |
| Molecular Weight | 202.3352 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Constitutive emission of the aphid alarm pheromone, (E)-β-farnesene, from plants does not serve as a direct defense against aphids. | 2010-11-23 |
|
| Antibacterial activities of a new brominated diterpene from Borneon Laurencia spp. | 2010-05-26 |
|
| The nature and fate of natural resins in the geosphere. XII. Investigation of C-ring aromatic diterpenoids in Raritan amber by pyrolysis-GC-matrix isolation FTIR-MS. | 2006-03-01 |
|
| Photomediated asymmetric synthesis of (-)-cuparene. | 2003-05-07 |
|
| Use of aromatic radical-anions in the absence of THF. Tandem formation and cyclization of benzyllithiums derived from the attack of homo- and bishomoallyllithiums on alpha-methylstyrenes: two-pot synthesis of cuparene. | 2001-04-18 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:45:24 GMT 2025
by
admin
on
Mon Mar 31 19:45:24 GMT 2025
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| Record UNII |
24IR5X2B93
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| Record Status |
Validated (UNII)
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| Record Version |
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