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Details

Stereochemistry RACEMIC
Molecular Formula C10H16
Molecular Weight 136.234
Optical Activity ( + / - )
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 3-CARENE

SMILES

CC1=CC[C@H]2[C@@H](C1)C2(C)C

InChI

InChIKey=BQOFWKZOCNGFEC-DTWKUNHWSA-N
InChI=1S/C10H16/c1-7-4-5-8-9(6-7)10(8,2)3/h4,8-9H,5-6H2,1-3H3/t8-,9+/m0/s1

HIDE SMILES / InChI

Molecular Formula C10H16
Molecular Weight 136.234
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Structural elucidation of monoterpene oxidation products by ion trap fragmentation using on-line atmospheric pressure chemical ionisation mass spectrometry in the negative ion mode.
2001
Airborne chemical compounds on dairy farms.
2001 Feb
Modeling the formation of secondary organic aerosol (SOA). 2. The predicted effects of relative humidity on aerosol formation in the alpha-pinene-, beta-pinene-, sabinene-, delta 3-carene-, and cyclohexene-ozone systems.
2001 May 1
Volatile metabolites from microorganisms grown on humid building materials and synthetic media.
2002 Oct
OH-initiated oxidation of monoterpenes: reaction of alpha-pinene.
2003 Apr
Mono and diterpene production in Escherichia coli.
2004 Jul 20
Contributions of organic peroxides to secondary aerosol formed from reactions of monoterpenes with O3.
2005 Jun 1
Inhibition of acetylcholinesterase activity by bicyclic monoterpenoids.
2005 Mar 9
Atmospheric fate of OH initiated oxidation of terpenes. Reaction mechanism of alpha-pinene degradation and secondary organic aerosol formation.
2005 May
[Analysis of volatile constituents in leaves of three cypress species by gas chromatography/mass spectrometry].
2006 Mar
Host selection in Tomicus piniperda L.: composition of monoterpene hydrocarbons in relation to attack frequency in the shoot feeding phase.
2006 May-Jun
Cross-attraction between an exotic and a native pine bark beetle: a novel invasion mechanism?
2007 Dec 12
Traps and attractants for wood-boring insects in ponderosa pine stands in the Black Hills, South Dakota.
2008 Apr
Synergistic blends of monoterpenes for aggregation pheromones of the mountain pine beetle (Coleoptera: Curculionidae).
2008 Aug
Mechanisms for the formation of organic acids in the gas-phase ozonolysis of 3-carene.
2009 Jun 7
Formaldehyde in the indoor environment.
2010 Apr 14
Complex interactions among host pines and fungi vectored by an invasive bark beetle.
2010 Aug
A facile and efficient synthesis of 3,3-dimethyl isopropylidene proline from (+)-3-carene.
2010 Feb 19
Genetics, phosphorus availability, and herbivore-derived induction as sources of phenotypic variation of leaf volatile terpenes in a pine species.
2010 Oct
Substance Class Chemical
Created
by admin
on Sat Dec 17 07:36:15 UTC 2022
Edited
by admin
on Sat Dec 17 07:36:15 UTC 2022
Record UNII
H2M15SNR6N
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
3-CARENE
FHFI   MI  
Systematic Name English
.DELTA.3-CARENE
Common Name English
3-KAREN
Common Name English
BICYCLO(4.1.0)HEPT-3-ENE, 3,7,7-TRIMETHYL-
Systematic Name English
3-CARENE [MI]
Common Name English
3-CARENE [FHFI]
Common Name English
(±)-.DELTA.3-CARENE
Common Name English
3-NORCARENE, 3,7,7-TRIMETHYL-
Systematic Name English
3,7,7-TRIMETHYLBICYCLO(4.1.0)HEPT-3-ENE
Systematic Name English
S-3-CARENE
Common Name English
FEMA NO. 3821
Code English
(±)-3-CARENE
Systematic Name English
Code System Code Type Description
DAILYMED
H2M15SNR6N
Created by admin on Sat Dec 17 07:36:15 UTC 2022 , Edited by admin on Sat Dec 17 07:36:15 UTC 2022
PRIMARY
RXCUI
2395760
Created by admin on Sat Dec 17 07:36:15 UTC 2022 , Edited by admin on Sat Dec 17 07:36:15 UTC 2022
PRIMARY
CHEBI
35661
Created by admin on Sat Dec 17 07:36:15 UTC 2022 , Edited by admin on Sat Dec 17 07:36:15 UTC 2022
PRIMARY
MERCK INDEX
M3105
Created by admin on Sat Dec 17 07:36:15 UTC 2022 , Edited by admin on Sat Dec 17 07:36:15 UTC 2022
PRIMARY Merck Index
WIKIPEDIA
3-Carene
Created by admin on Sat Dec 17 07:36:15 UTC 2022 , Edited by admin on Sat Dec 17 07:36:15 UTC 2022
PRIMARY
FDA UNII
H2M15SNR6N
Created by admin on Sat Dec 17 07:36:15 UTC 2022 , Edited by admin on Sat Dec 17 07:36:15 UTC 2022
PRIMARY
CAS
13466-78-9
Created by admin on Sat Dec 17 07:36:15 UTC 2022 , Edited by admin on Sat Dec 17 07:36:15 UTC 2022
PRIMARY
MESH
C030218
Created by admin on Sat Dec 17 07:36:15 UTC 2022 , Edited by admin on Sat Dec 17 07:36:15 UTC 2022
PRIMARY
EPA CompTox
DTXSID4047462
Created by admin on Sat Dec 17 07:36:15 UTC 2022 , Edited by admin on Sat Dec 17 07:36:15 UTC 2022
PRIMARY
ECHA (EC/EINECS)
236-719-3
Created by admin on Sat Dec 17 07:36:15 UTC 2022 , Edited by admin on Sat Dec 17 07:36:15 UTC 2022
PRIMARY
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