Results for:
PubChem ID: 7460

2-methyl-5-propan-2-ylcyclohexa-1,3-diene

Mass-Spectra

Compound Details

Synonymous names	Isopropylmethylcyclohexane, tetradehydro derivative PHELLANDRENE Menthadiene alpha-Fellandrene PHELLANDRENE,ALPHA alpha Phellandrene alpha-Phellandren OGLDWXZKYODSOB-UHFFFAOYSA-N ALPHA-PHELLANDRENE MENTHANE TETRADEHYDRO DERIVATIVE Menthane, tetradehydro derivative a-phellandrene 1-phellandrene Dihydro-p-cymene .alpha.-Phellandrene AC1L1OT7 alpha-Phellandrene (natural) .alpha.-Fellandrene AC1Q29WV Phellandrene, alpha- 5731AF NSC1842 CTK3J3667 M0051 ACMC-209t0j HSDB 1130 DTXSID4047593 CHEMBL3188459 LS-3023 NSC-1842 OR038356 OR213985 OR260482 CHEBI:50035 ANW-41873 AN-24525 DSSTox_GSID_47593 (-)-??-Phellandrene p-Mentha-1,5-diene MFCD00040419 C-54386 DSSTox_RID_82440 DSSTox_CID_27593 TR-030690 RTR-030690 DB-070271 AKOS015913085 FT-0607984 FEMA No. 2856 BRN 1280394 99-83-2 5-Isopropyl-2-methyl-1,3-cyclohexadiene 1-Methyl-4-isopropyl-1,5-cyclohexadiene I14-46722 2-Methyl-5-isopropyl-1,3-cyclohexadien 1-Isopropyl-4-methyl-2,4-cyclohexadiene 2-Methyl-5-isopropyl-1,3-cyclohexadiene alpha-Phellandrene, natural, >=85%, FG 5-isopropyl-2-methylcyclohexa-1,3-diene 4-Isopropyl-1-methyl-1,5-cyclohexadiene Tox21_302550 (+)-.alpha.-phellandrene CAS-99-83-2 5-isopropyl-2-methyl-cyclohexa-1,3-diene NCGC00256667-01 1330-17-2 1329-99-3 4221-98-1 EINECS 252-034-2 EINECS 215-532-0 EINECS 202-792-5 13811-01-3 25377-78-0 2-methyl-5-propan-2-ylcyclohexa-1,3-diene (-)-p-Mentha-1,5-diene 2-methyl-5-(1-methylethyl)-1,3-cyclohexadiene (-)-5-Isopropyl-2-methyl-1,3-cyclohexadiene Cyclohexane, 1-methyl-4-(1-methylethyl)-, tetradehydro deriv. 2-methyl-5-(propan-2-yl)cyclohexa-1,3-diene 3-05-00-00342 (Beilstein Handbook Reference) 1,3-Cyclohexadiene, 2-methyl-5-(1-methylethyl)- (-)-2-Methyl-5-(1-methylethyl)-1,3-cyclohexadiene 1,3-Cyclohexadiene, 2-methyl-5-(1-methylethyl)-, (R)- 1,3-Cyclohexadiene, 2-methyl-5-(1-methylethyl)-, (5R)-
Microorganism:	Yes
IUPAC name	2-methyl-5-propan-2-ylcyclohexa-1,3-diene
SMILES	CC1=CCC(C=C1)C(C)C
Inchi	InChI=1S/C10H16/c1-8(2)10-6-4-9(3)5-7-10/h4-6,8,10H,7H2,1-3H3
Formula	C10H16
PubChem ID	7460
Molweight	136.238
LogP	3.21
Atoms	26
Bonds	26
H-bond Acceptor	0
H-bond Donor	0
Chemical Classification	Terpenes

mVOC Specific Details

MS-Links

MS-MS Spectrum 85596 MS-MS Spectrum 147728 MS-MS Spectrum 147726 MS-MS Spectrum 147727 MS-MS Spectrum 85598 MS-MS Spectrum 85597

Microorganisms emitting the compound

Kingdom Species Biological Function Origin/Habitat Reference Fungi Hypoxylon Antochroum Blaci na endophytic in Bursera lancifolia Ulloa-Benítez et al., 2016 Fungi Fusarium Culmorum PV na sandy dune soil, Netherlands Schmidt et al., 2016 Fungi Paecilomyces Variotii compost Fischer et al. 2046 Fungi Trichoderma Atroviride na water damaged buildings, Belgium Polizzi et al., 2012 Fungi Amanita Ovoidea France Breheret et al. 1997 Fungi Aspergillus Fumigatus Strain FGSC A1163 Heddergott et al. 2014 Fungi Trichoderma Atroviride ATCC 74058 n/a Stoppacher et al., 2010 Fungi Tuber Magnatum n/a Italian geographical areas (Emilia Romagna, Border region area between Emilia Romagna and Marche) Gioacchini et al., 2008

Method

Kingdom Species Growth Medium Applied Method Verification Fungi Hypoxylon Antochroum Blaci PDA/WA + 500 mg l^-1 Chloramphenicol SPME-GC/MS No Fungi Fusarium Culmorum PV water agar supplied with artificial root exudates GC/MS-Q-TOF No Fungi Paecilomyces Variotii yest extract sucrose Tenax/GC-MS no Fungi Trichoderma Atroviride malt extract agar; potato dextrose agar; water agar; yeast extract agar; Czapek agar SPME-GC/MS No Fungi Amanita Ovoidea forest soil solvent extraction, headspace, GCMS no Fungi Aspergillus Fumigatus Strain FGSC A1163 Brian`s broth, AMM, RPMI 1660 SPME / GC-MS Fungi Trichoderma Atroviride ATCC 74058 Potato dextrose agar HS-SPME/GC-MS Fungi Tuber Magnatum n/a microextraction-gas chromatography-mass spectrometry analysis (SPME-GC-MS)