Results for:
chemical Classification: alkatrienes

(3E)-3-prop-2-enylidenecyclobutene

Compound Details

Synonymous names
52097-85-5
Cyclobutene, 2-propenylidene-
(3E)-3-prop-2-enylidenecyclobutene
Cyclobutene, 3-(2-propen-1-ylidene)-
USDJJNZZCBONHN-DAXSKMNVSA-N
DB-247012
(3E)-3-(2-Propenylidene)-1-cyclobutene #
Microorganism:

Yes

IUPAC name(3E)-3-prop-2-enylidenecyclobutene
SMILESC=CC=C1CC=C1
InchiInChI=1S/C7H8/c1-2-4-7-5-3-6-7/h2-5H,1,6H2/b7-4-
FormulaC7H8
PubChem ID5368360
Molweight92.14
LogP2.1
Atoms7
Bonds1
H-bond Acceptor0
H-bond Donor0
Chemical Classificationalkatrienes unsaturated hydrocarbons
Supernatural-IDSN0378673-01

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaPseudomonas Putidanablack pepper rootSheoran et al. 2015
ProkaryotaPseudomonas Putidapositive influence of the plant root growth and protection against soil-borne pathogensNASheoran et al. 2015
Meyerozyma GuilliermondiiXiong et al. 2023
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaPseudomonas PutidaLuria Bertani AgarHeadspace GC/MSno
ProkaryotaPseudomonas PutidaTSBPropak Q adsorbent trap/GC-MSno
Meyerozyma GuilliermondiiYEPD, 10 g/L yeast extrac, 20 g/L peptone, 20 g dextroseGC-MS and GC-IMSno


(3E,5Z)-octa-1,3,5-triene

Compound Details

Synonymous names
fucoserratene
(3E,5Z)-octa-1,3,5-triene
1,3E,5Z-Octatriene
33580-05-1
Sarohornene C
1,3,5-Octatriene, (E,Z)-
1,3,5-Octatriene, (3E,5Z)-
3-trans,6-cis-octatriene
1,3-trans,5-cis-octatriene
(E,Z)-1,3,5-Octatriene
(3E,5Z)-1,3,5-Octatriene
1,3-(E)-5-(Z)-Octatriene
HOXGZVUCAYFWGR-YMBWGVAGSA-N
fucoserratene,(3E,5E)-1,3,5-octatriene,(E,Z)-1,3,5-octatriene
Microorganism:

No

IUPAC name(3E,5Z)-octa-1,3,5-triene
SMILESCCC=CC=CC=C
InchiInChI=1S/C8H12/c1-3-5-7-8-6-4-2/h3,5-8H,1,4H2,2H3/b7-5+,8-6-
FormulaC8H12
PubChem ID5367475
Molweight108.18
LogP3.8
Atoms8
Bonds3
H-bond Acceptor0
H-bond Donor0
Chemical Classificationalkatrienes unsaturated hydrocarbons
Supernatural-IDSN0131514-04

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaTrichoderma VirensNACrutcher et al. 2013
EukaryotaTrichoderma AtrovirideNACrutcher et al. 2013
EukaryotaTrichoderma ReeseiNACrutcher et al. 2013
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaTrichoderma VirensPotato dextrose agarHS-SPME/GC-MS no
EukaryotaTrichoderma AtroviridePotato dextrose agarHS-SPME/GC-MS no
EukaryotaTrichoderma ReeseiPotato dextrose agarHS-SPME/GC-MS no


(3E,5E)-hepta-1,3,5-triene

Mass-Spectra

Compound Details

Synonymous names
1,3,5-Heptatriene
17679-93-5
(3E,5E)-hepta-1,3,5-triene
trans,trans-1,3,5-Heptatriene
1,3,5-Heptatriene, (E,E)-
(E,E)-1,3,5-heptatriene
All-trans-1,3,5-Heptatriene
(3E,5E)-1,3,5-Heptatriene
1,3,5-Heptatriene,(3E,5E)-
heptatriene
2196-23-8
CHEBI:177462
USKZHEQYENVSMH-UHFFFAOYSA-N
USKZHEQYENVSMH-YDFGWWAZSA-N
DTXSID001015939
(E,E)-CH2=CHCH=CHCH=CHCH3
Microorganism:

No

IUPAC name(3E,5E)-hepta-1,3,5-triene
SMILESCC=CC=CC=C
InchiInChI=1S/C7H10/c1-3-5-7-6-4-2/h3-7H,1H2,2H3/b6-4+,7-5+
FormulaC7H10
PubChem ID5367390
Molweight94.15
LogP3
Atoms7
Bonds2
H-bond Acceptor0
H-bond Donor0
Chemical Classificationalkatrienes unsaturated hydrocarbons
CHEBI-ID177462

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaNigrograna MackinnoniiNAShaw et al. 2015
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaNigrograna Mackinnoniino


(3E,6E)-octa-1,3,6-triene

Mass-Spectra

Compound Details

Synonymous names
1,3,6-Octatriene
(3E,6E)-octa-1,3,6-triene
22038-69-3
octa-1,3,6-triene
CHEBI:216494
PKHBEGZTQNOZLP-YDFGWWAZSA-N
1,3,6-OCTATRIENE (E,E)
Microorganism:

No

IUPAC name(3E,6E)-octa-1,3,6-triene
SMILESCC=CCC=CC=C
InchiInChI=1S/C8H12/c1-3-5-7-8-6-4-2/h3-7H,1,8H2,2H3/b6-4+,7-5+
FormulaC8H12
PubChem ID5367382
Molweight108.18
LogP3
Atoms8
Bonds3
H-bond Acceptor0
H-bond Donor0
Chemical Classificationalkatrienes unsaturated hydrocarbons
CHEBI-ID216494
Supernatural-IDSN0287686-01

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaAspergillus Candiduscompost Fischer et al. 1999
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaAspergillus Candidusyest extract sucroseTenax/GC-MSno


(3E)-4,8-dimethylnona-1,3,7-triene

Compound Details

Synonymous names
19945-61-0
(E)-4,8-Dimethyl-1,3,7-nonatriene
(3E)-4,8-dimethylnona-1,3,7-triene
(3E)-4,8-dimethyl-1,3,7-nonatriene
4,8-Dimethylnona-1,3,7-triene
51911-82-1
1,3,7-Nonatriene, 4,8-dimethyl-, (3E)-
4,8-dimethyl-1,3(E),7-nonatriene
(e)-4,8-dimethylnona-1,3,7-triene
4,8-Dimethyl-1,3E,7-nonatriene
e-4,8-dimethyl-1,3,7-nonatriene
1,3,7-Nonatriene, 4,8-dimethyl-, (E)-
CHEBI:60158
2,6-dimethyl-2,6,8-nonatriene
DTXSID201304588
LMFA11000037
1,3,7-Nonatriene, 4,8-dimethyl-,
(3E)-4,8-dimethyl-nona-1,3,7-triene
(E)-4,8-Dimethylnona-1, 3, 7-triene
DB-309887
CS-0224691
C21795
EN300-120476
G76818
A828848
A929243
Q27127102
Microorganism:

Yes

IUPAC name(3E)-4,8-dimethylnona-1,3,7-triene
SMILESCC(=CCCC(=CC=C)C)C
InchiInChI=1S/C11H18/c1-5-7-11(4)9-6-8-10(2)3/h5,7-8H,1,6,9H2,2-4H3/b11-7+
FormulaC11H18
PubChem ID6427110
Molweight150.26
LogP4.6
Atoms11
Bonds4
H-bond Acceptor0
H-bond Donor0
Chemical Classificationalkatrienes terpenes unsaturated hydrocarbons
CHEBI-ID60158
Supernatural-IDSN0215712-01

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaStreptomyces Caviscabiesn/aNASchulz and Dickschat 2007
ProkaryotaStreptomyces Sp.n/aNADickschat et al. 2005_2
EukaryotaCryptococcus NemorosusNANALjunggren et al. 2019
EukaryotaMetschnikowia AndauensisNANALjunggren et al. 2019
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaStreptomyces Caviscabiesn/an/ano
ProkaryotaStreptomyces Sp.n/an/ano
EukaryotaCryptococcus Nemorosusliquid YPD mediumGC-MSno
EukaryotaMetschnikowia Andauensisliquid YPD mediumGC-MSno