Results for:
chemical Classification: azides

2,6-bis[(4-azidophenyl)methylidene]cyclohexan-1-one

Compound Details

Synonymous names
20237-98-3
2,6-bis[(4-azidophenyl)methylidene]cyclohexan-1-one
Cyclohexanone, 2,6-bis[(4-azidophenyl)methylene]-
2,6-Bis(p-azidobenzylidene)cyclohexanone
Cyclohexanone, 2,6-bis((4-azidophenyl)methylene)-
EINECS 243-625-6
2,6-Di(4'-azidobenzylidene)cyclohexanone
2,6-Bis(4-azidobenzylidene)cyclohexan-1-one
DTXSID1066574
UZNOMHUYXSAUPB-UHFFFAOYSA-N
2,6-bis-(4'-azidobenzal)-cyclohexanone
NS00026553
Microorganism:

Yes

IUPAC name2,6-bis[(4-azidophenyl)methylidene]cyclohexan-1-one
SMILESC1CC(=CC2=CC=C(C=C2)N=[N+]=[N-])C(=O)C(=CC3=CC=C(C=C3)N=[N+]=[N-])C1
InchiInChI=1S/C20H16N6O/c21-25-23-18-8-4-14(5-9-18)12-16-2-1-3-17(20(16)27)13-15-6-10-19(11-7-15)24-26-22/h4-13H,1-3H2
FormulaC20H16N6O
PubChem ID89294
Molweight356.4
LogP6.9
Atoms27
Bonds4
H-bond Acceptor5
H-bond Donor0
Chemical Classificationnitrogen compounds ketones benzenoids azides aromatic compounds

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
Pectobacterium CarotovorumKate et al. 2023
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
Pectobacterium Carotovoruminoculated potato samplesGC-MSno


Azidomethylbenzene

Compound Details

Synonymous names
Benzyl azide
(Azidomethyl)benzene
622-79-7
Benzylazide
azidomethylbenzene
Benzene, (azidomethyl)-
alpha-Azidotoluene
Toluene, .alpha.-azido-
Benzyl Azide, Pract.
Triazotoluene
azidomethyl-benzene
.alpha.-Azidotoluene
HFD57Z7J9J
CHEMBL3236190
MFCD00013836
NSC-26304
Benzene, azidomethyl-
NSC 26304
CCRIS 8029
UNII-HFD57Z7J9J
TOLUENE, alpha-AZIDO-
BRN 1907583
a-Azidotoluene
(azidomethyl) benzene
Toluene, alpha-triazo-
Bn-N3
WLN: NNNR B1
(Azidomethyl)benzene, Pract.
4-05-00-00877 (Beilstein Handbook Reference)
LCZC2717
SCHEMBL13437571
DTXSID90211244
AMY19781
NSC26304
BDBM50573332
STL192368
AKOS005166902
AT41578
FS-5590
SY040161
DB-054116
EN300-82312
10.14272/UDLLFLQFQMACJB-UHFFFAOYSA-N.1
doi:10.14272/UDLLFLQFQMACJB-UHFFFAOYSA-N.1
Q13438697
F1905-6985
Microorganism:

No

IUPAC nameazidomethylbenzene
SMILESC1=CC=C(C=C1)CN=[N+]=[N-]
InchiInChI=1S/C7H7N3/c8-10-9-6-7-4-2-1-3-5-7/h1-5H,6H2
FormulaC7H7N3
PubChem ID12152
Molweight133.15
LogP2.8
Atoms10
Bonds2
H-bond Acceptor2
H-bond Donor0
Chemical Classificationnitrogen compounds benzenoids azides aromatic compounds

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
Aspergillus NigerKate et al. 2023
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
Aspergillus Nigerinoculated potato samplesGC-MSno


3-azidoprop-1-ene

Compound Details

Synonymous names
3-azidoprop-1-ene
1-Propene, 3-azido-
821-13-6
allyl azide
DTXSID00336391
VYZOFUACMOJPRL-UHFFFAOYSA-N
EN300-256043
Microorganism:

Yes

IUPAC name3-azidoprop-1-ene
SMILESC=CCN=[N+]=[N-]
InchiInChI=1S/C3H5N3/c1-2-3-5-6-4/h2H,1,3H2
FormulaC3H5N3
PubChem ID533456
Molweight83.09
LogP1.9
Atoms6
Bonds2
H-bond Acceptor2
H-bond Donor0
Chemical Classificationazides nitrogen compounds

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
Pectobacterium CarotovorumKate et al. 2023
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
Pectobacterium Carotovoruminoculated potato samplesGC-MSno


Bis(3-azido-4-methoxyphenyl)methanone

Compound Details

Synonymous names
Bis-(3-azido-4-methoxy-phenyl)methanone
YTFPVGLVSMVYBP-UHFFFAOYSA-N
Microorganism:

Yes

IUPAC namebis(3-azido-4-methoxyphenyl)methanone
SMILESCOC1=C(C=C(C=C1)C(=O)C2=CC(=C(C=C2)OC)N=[N+]=[N-])N=[N+]=[N-]
InchiInChI=1S/C15H12N6O3/c1-23-13-5-3-9(7-11(13)18-20-16)15(22)10-4-6-14(24-2)12(8-10)19-21-17/h3-8H,1-2H3
FormulaC15H12N6O3
PubChem ID533554
Molweight324.29
LogP5.1
Atoms24
Bonds6
H-bond Acceptor7
H-bond Donor0
Chemical Classificationaromatic compounds aromatic ketones azides benzenoids ethers ketones nitrogen compounds

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
Pectobacterium CarotovorumKate et al. 2023
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
Pectobacterium Carotovoruminoculated potato samplesGC-MSno


(2E,6E)-2,6-bis[(4-azidophenyl)methylidene]-4-methylcyclohexan-1-one

Compound Details

Synonymous names
2,6-Bis(4-azidobenzylidene)-4-methylcyclohexanone
2,6-Bis(4-azidobenzylidene)-4-methylcyclohexan-1-one
2,6-di(p-Azidobenzal)-4-methylcyclohexanone
2,6-Di(4-azidobenzal)-4-methylcyclohexanone
2,6-Bis[(4-azidophenyl)methylene]-4-methylcyclohexanone
SV8HZ947ZU
MLIWQXBKMZNZNF-PWDIZTEBSA-N
AKOS015853832
A-016
B1111
2,6-bis(4-azidobenzal)-4-methylcyclohexanone
2,6-Bis(p-azidobenzal)-4-methylcyclohexanone
2,6-Bis(p-azidobenzylidene)-4-methylcyclohexanone
2,6-di(4-azidobenzylidene)-4-methylcyclohexanone
2,6-Bis(4'-azidobenzylidene)-4-methylcyclohexanone
1,3-Bis(p-azidobenzylidene)-5-methylcyclohexan-2-one
4-Methyl-2,6-bis(4'-azidobenzylidene)cyclohexan-1-one
2,6-Bis(4-azidobenzylidene)-4-methylcyclohexanone, contains 20-45% water as stabilizer, 97%
Microorganism:

Yes

IUPAC name(2E,6E)-2,6-bis[(4-azidophenyl)methylidene]-4-methylcyclohexan-1-one
SMILESCC1CC(=CC2=CC=C(C=C2)N=[N+]=[N-])C(=O)C(=CC3=CC=C(C=C3)N=[N+]=[N-])C1
InchiInChI=1S/C21H18N6O/c1-14-10-17(12-15-2-6-19(7-3-15)24-26-22)21(28)18(11-14)13-16-4-8-20(9-5-16)25-27-23/h2-9,12-14H,10-11H2,1H3/b17-12+,18-13+
FormulaC21H18N6O
PubChem ID5466536
Molweight370.4
LogP7.2
Atoms28
Bonds4
H-bond Acceptor5
H-bond Donor0
Chemical Classificationaromatic compounds azides benzenoids ketones nitrogen compounds

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
Aspergillus FlavusKate et al. 2023
Pectobacterium CarotovorumKate et al. 2023
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
Aspergillus Flavusinoculated potato samplesGC-MSno
Pectobacterium Carotovoruminoculated potato samplesGC-MSno