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 |
---|---|---|
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 Apr 18 |
|
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 Mar 1 |
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Antibacterial activities of a new brominated diterpene from Borneon Laurencia spp. | 2010 May 26 |
|
Constitutive emission of the aphid alarm pheromone, (E)-β-farnesene, from plants does not serve as a direct defense against aphids. | 2010 Nov 23 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 19:28:58 GMT 2023
by
admin
on
Fri Dec 15 19:28:58 GMT 2023
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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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-
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