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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
Structure of CUPARENE

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

HIDE SMILES / InChI

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

PubMed

TitleDatePubMed
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
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 Fri Dec 15 19:28:58 GMT 2023
Edited
by admin
on Fri Dec 15 19:28:58 GMT 2023
Record UNII
24IR5X2B93
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CUPARENE
Common Name English
(R)-1-METHYL-4-(1,2,2-TRIMETHYLCYCLOPENTYL)BENZENE
Systematic Name English
TOLUENE, P-(1,2,2-TRIMETHYLCYCLOPENTYL)-, (R)-(+)-
Common Name English
BENZENE, 1-METHYL-4-(1,2,2-TRIMETHYLCYCLOPENTYL)-, (.THETA.)-
Systematic Name English
(R)-CUPARENE
Common Name English
BENZENE, 1-METHYL-4-(1,2,2-TRIMETHYLCYCLOPENTYL)-, (R)-
Common Name English
CUPARENE, (+)-
Common Name English
(+)-CUPARENE
Common Name English
(R)-(+)-P-(1,2,2-TRIMETHYLCYCLOPENTYL)TOLUENE
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID70168762
Created by admin on Fri Dec 15 19:28:58 GMT 2023 , Edited by admin on Fri Dec 15 19:28:58 GMT 2023
PRIMARY
FDA UNII
24IR5X2B93
Created by admin on Fri Dec 15 19:28:58 GMT 2023 , Edited by admin on Fri Dec 15 19:28:58 GMT 2023
PRIMARY
ECHA (EC/EINECS)
241-061-5
Created by admin on Fri Dec 15 19:28:58 GMT 2023 , Edited by admin on Fri Dec 15 19:28:58 GMT 2023
PRIMARY
CAS
16982-00-6
Created by admin on Fri Dec 15 19:28:58 GMT 2023 , Edited by admin on Fri Dec 15 19:28:58 GMT 2023
PRIMARY
PUBCHEM
86895
Created by admin on Fri Dec 15 19:28:58 GMT 2023 , Edited by admin on Fri Dec 15 19:28:58 GMT 2023
PRIMARY