3-CARENE

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 Search

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

Title	Date	PubMed
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	11746892
Airborne chemical compounds on dairy farms.	2001 Feb	11354733
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	11355196
Volatile metabolites from microorganisms grown on humid building materials and synthetic media.	2002 Oct	12400912
OH-initiated oxidation of monoterpenes: reaction of alpha-pinene.	2003 Apr	12817640
Mono and diterpene production in Escherichia coli.	2004 Jul 20	15236249
Contributions of organic peroxides to secondary aerosol formed from reactions of monoterpenes with O3.	2005 Jun 1	15984782
Inhibition of acetylcholinesterase activity by bicyclic monoterpenoids.	2005 Mar 9	15740071
Atmospheric fate of OH initiated oxidation of terpenes. Reaction mechanism of alpha-pinene degradation and secondary organic aerosol formation.	2005 May	15829369
[Analysis of volatile constituents in leaves of three cypress species by gas chromatography/mass spectrometry].	2006 Mar	16830472
Host selection in Tomicus piniperda L.: composition of monoterpene hydrocarbons in relation to attack frequency in the shoot feeding phase.	2006 May-Jun	16869505
Cross-attraction between an exotic and a native pine bark beetle: a novel invasion mechanism?	2007 Dec 12	18074026
Traps and attractants for wood-boring insects in ponderosa pine stands in the Black Hills, South Dakota.	2008 Apr	18459406
Synergistic blends of monoterpenes for aggregation pheromones of the mountain pine beetle (Coleoptera: Curculionidae).	2008 Aug	18767736
Mechanisms for the formation of organic acids in the gas-phase ozonolysis of 3-carene.	2009 Jun 7	19458820
Formaldehyde in the indoor environment.	2010 Apr 14	20067232
Complex interactions among host pines and fungi vectored by an invasive bark beetle.	2010 Aug	20546136
A facile and efficient synthesis of 3,3-dimethyl isopropylidene proline from (+)-3-carene.	2010 Feb 19	20108962
Genetics, phosphorus availability, and herbivore-derived induction as sources of phenotypic variation of leaf volatile terpenes in a pine species.	2010 Oct	20952630

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

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Name

Type

Language

3-CARENE

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