U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C15H24
Molecular Weight 204.3511
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LONGIFOLENE

SMILES

C[C@]12CCCC(C)(C)[C@H]3[C@H](CC[C@@H]13)C2=C

InChI

InChIKey=PDSNLYSELAIEBU-GUIRCDHDSA-N
InChI=1S/C15H24/c1-10-11-6-7-12-13(11)14(2,3)8-5-9-15(10,12)4/h11-13H,1,5-9H2,2-4H3/t11-,12-,13+,15-/m1/s1

HIDE SMILES / InChI

Molecular Formula C15H24
Molecular Weight 204.3511
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 4 / 4
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Phytotoxic volatiles in the roots and shoots of Artemisia tridentata as detected by headspace solid-phase microextraction and gas chromatographic-mass spectrometry analysis.
2010-12
Subgroup 4 R2R3-MYBs in conifer trees: gene family expansion and contribution to the isoprenoid- and flavonoid-oriented responses.
2010-09
Comparative analysis of essential oil components of two Pinus species from Taibai Mountain in China.
2010-08
Antimycobacterial terpenoids from Juniperus communis L. (Cuppressaceae).
2009-12-10
[Study on chemical constituents from essential oil of Hypericum patulum].
2009-02
Does egg deposition by herbivorous pine sawflies affect transcription of sesquiterpene synthases in pine?
2008-08
Chemotaxis of the pinewood nematode, Bursaphelenchus xylophilus, to volatiles associated with host pine, Pinus massoniana, and its vector Monochamus alternatus.
2007-06
Solution conformation of longifolene and its precursor by NMR and ab initio calculations.
2006-12
Trypanocidal activity of oleoresin and terpenoids isolated from Pinus oocarpa.
2005-12-03
Vegetation-derived cues for the selection of oviposition substrates by Anopheles albimanus under laboratory conditions.
2005-12
Flavor characteristics of lapsang souchong and smoked lapsang souchong, a special Chinese black tea with pine smoking process.
2005-11-02
Changes in anatomy and terpene chemistry in roots of Douglas-fir seedlings following treatment with methyl jasmonate.
2005-08
The cationic cascade route to longifolene.
2005-06-24
[Allelopathic effects of Cymbopogon citratu volatile and its chemical components].
2005-04
New woody and ambery notes from cedarwood and turpentine oil.
2004-12
An efficient formal synthesis of the sesquiterpenoid longifolene.
2003-04
[Analysis of terpineol and improvement of technology process in terpineol production].
2002-11
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:02:22 GMT 2025
Edited
by admin
on Mon Mar 31 18:02:22 GMT 2025
Record UNII
3YXH7YY8WM
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LONGIFOLENE
INCI   MI  
INCI  
Official Name English
NSC-150808
Preferred Name English
(1S-(1.ALPHA.,3A.BETA.,4.ALPHA.,8A.BETA.))DECAHYDRO-4,8,8-TRIMETHYL-9-METHYLENE-1,4-METHANOAZULENE
Common Name English
.ALPHA.-LONGIFOLENE
Common Name English
1,4-METHANOAZULENE, DECAHYDRO-4,8,8-TRIMETHYL-9-METHYLENE-, (1S,3AR,4S,8AS)-
Common Name English
JUNIPENE
Common Name English
(+)-LONGIFOLENE
Common Name English
LONGIFOLENE [MI]
Common Name English
1,4-METHANOAZULENE, DECAHYDRO-4,8,8-TRIMETHYL-9-METHYLENE-, (1S-(1.ALPHA.,3A.BETA.,4.ALPHA.,8A.BETA.))-
Common Name English
KUROMATSUENE
Common Name English
D-LONGIFOLENE
Common Name English
1,4-METHANOAZULENE, DECAHYDRO-4,8,8-TRIMETHYL-9-METHYLENE-, (1S,3AR,4S,8AS)-(+)-
Common Name English
JUNIPEN
Common Name English
KUROMATSUEN
Common Name English
LONGIFOLEN
Common Name English
Code System Code Type Description
CAS
475-20-7
Created by admin on Mon Mar 31 18:02:22 GMT 2025 , Edited by admin on Mon Mar 31 18:02:22 GMT 2025
PRIMARY
CHEBI
49282
Created by admin on Mon Mar 31 18:02:22 GMT 2025 , Edited by admin on Mon Mar 31 18:02:22 GMT 2025
PRIMARY
EPA CompTox
DTXSID9047045
Created by admin on Mon Mar 31 18:02:22 GMT 2025 , Edited by admin on Mon Mar 31 18:02:22 GMT 2025
PRIMARY
FDA UNII
3YXH7YY8WM
Created by admin on Mon Mar 31 18:02:22 GMT 2025 , Edited by admin on Mon Mar 31 18:02:22 GMT 2025
PRIMARY
PUBCHEM
1796220
Created by admin on Mon Mar 31 18:02:22 GMT 2025 , Edited by admin on Mon Mar 31 18:02:22 GMT 2025
PRIMARY
MERCK INDEX
m6894
Created by admin on Mon Mar 31 18:02:22 GMT 2025 , Edited by admin on Mon Mar 31 18:02:22 GMT 2025
PRIMARY Merck Index
CHEBI
6530
Created by admin on Mon Mar 31 18:02:22 GMT 2025 , Edited by admin on Mon Mar 31 18:02:22 GMT 2025
PRIMARY
ECHA (EC/EINECS)
207-491-2
Created by admin on Mon Mar 31 18:02:22 GMT 2025 , Edited by admin on Mon Mar 31 18:02:22 GMT 2025
PRIMARY
NSC
150808
Created by admin on Mon Mar 31 18:02:22 GMT 2025 , Edited by admin on Mon Mar 31 18:02:22 GMT 2025
PRIMARY
WIKIPEDIA
LONGIFOLENE
Created by admin on Mon Mar 31 18:02:22 GMT 2025 , Edited by admin on Mon Mar 31 18:02:22 GMT 2025
PRIMARY