Results for:
chemical Classification: azides

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:

IUPAC name

azidomethylbenzene

SMILES

C1=CC=C(C=C1)CN=[N+]=[N-]

Inchi

InChI=1S/C7H7N3/c8-10-9-6-7-4-2-1-3-5-7/h1-5H,6H2

Formula

C₇H₇N₃

PubChem ID

12152

Molweight

133.15

LogP

2.8

Atoms

Bonds

H-bond Acceptor

H-bond Donor

Chemical Classification

nitrogen compounds benzenoids azides aromatic compounds

mVOC Specific Details

Species emitting the compound

Kingdom	Species	Biological Function	Origin/Habitat	Reference
	Aspergillus Niger			Kate et al. 2023

Method

Kingdom	Species	Growth Medium	Applied Method	Verification
	Aspergillus Niger	inoculated potato samples	GC-MS	no

1,3-diaminourea

Compound Details

Synonymous names

Carbohydrazide

497-18-7

Carbonic dihydrazide

1,3-Diaminourea

Carbonohydrazide

Carbazide

Carbodihydrazide

Hydrazine, carbonyldi-

Hydrazine, carbonylbis-

Carbazic acid, hydrazide

carbonyl dihydrazine

Semicarbazide, 4-amino-

Carbonic acid, dihydrazide

Cabazide

Karbazid

Hydrazinecarboxamide, N-amino-

Urea, 1,3-diamino-

Urea, N,N'-diamino-

Hydrazinecarboxylic acid, hydrazide

1,3-Diaminomocovina

Carbonohydrazid

carbonodihydrazide

NSC 1934

N,N'-diaminourea

4-aminosemicarbazide

carbonylbis-hydrazine

hydrazinecarbohydrazide

N-aminohydrazinecarboxamide

W8V7FYY4WH

N-aminohydrazine carboxamide

hydrazide hydrazinecarboxylic acid

NSC-1934

Karbazid [Czech]

CH6N4O

1,3-Diaminomocovina [Czech]

EINECS 207-837-2

UNII-W8V7FYY4WH

BRN 1747069

AI3-52397

carbonyldihydrazide

Urea,3-diamino-

Urea,N'-diamino-

Carbohydrazide, 98%

1,3-bis(azanyl)urea

WLN: ZMVMZ

CARBOHYDRAZIDE [MI]

EC 207-837-2

4-03-00-00240 (Beilstein Handbook Reference)

DTXSID5038757

CHEBI:61308

NSC1934

O C (N H N H2)2

AMY40845

MFCD00007591

AKOS003193931

DB-029568

CS-0149890

NS00001612

EN300-20051

E77171

A827826

Q5037885

W-106011

Microorganism:

IUPAC name

1,3-diaminourea

SMILES

C(=O)(NN)NN

Inchi

InChI=1S/CH6N4O/c2-4-1(6)5-3/h2-3H2,(H2,4,5,6)

Formula

CH₆N₄O

PubChem ID

73948

Molweight

90.09

LogP

-1.6

Atoms

Bonds

H-bond Acceptor

H-bond Donor

Chemical Classification

nitrogen compounds hydrazides

CHEBI-ID

61308

mVOC Specific Details

Massbank-Links

Massbank Spectrum MSBNK-Fac_Eng_Univ_Tokyo-JP009979

Species emitting the compound

Kingdom	Species	Biological Function	Origin/Habitat	Reference
	Aspergillus Niger			Kate et al. 2023

Method

Kingdom	Species	Growth Medium	Applied Method	Verification
	Aspergillus Niger	inoculated potato samples	GC-MS	no

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 name

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

SMILES

C1CC(=CC2=CC=C(C=C2)N=[N+]=[N-])C(=O)C(=CC3=CC=C(C=C3)N=[N+]=[N-])C1

Inchi

InChI=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

Formula

C₂₀H₁₆N₆O

PubChem ID

89294

Molweight

356.4

LogP

6.9

Atoms

Bonds

H-bond Acceptor

H-bond Donor

Chemical Classification

nitrogen compounds ketones benzenoids azides aromatic compounds

mVOC Specific Details

Species emitting the compound

Kingdom	Species	Biological Function	Origin/Habitat	Reference
	Pectobacterium Carotovorum			Kate et al. 2023

Method

Kingdom	Species	Growth Medium	Applied Method	Verification
	Pectobacterium Carotovorum	inoculated potato samples	GC-MS	no

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 name

3-azidoprop-1-ene

SMILES

C=CCN=[N+]=[N-]

Inchi

InChI=1S/C3H5N3/c1-2-3-5-6-4/h2H,1,3H2

Formula

C₃H₅N₃

PubChem ID

533456

Molweight

83.09

LogP

1.9

Atoms

Bonds

H-bond Acceptor

H-bond Donor

Chemical Classification

azides nitrogen compounds

mVOC Specific Details

Species emitting the compound

Kingdom	Species	Biological Function	Origin/Habitat	Reference
	Pectobacterium Carotovorum			Kate et al. 2023

Method

Kingdom	Species	Growth Medium	Applied Method	Verification
	Pectobacterium Carotovorum	inoculated potato samples	GC-MS	no

Bis(3-azido-4-methoxyphenyl)methanone

Compound Details

Synonymous names

Bis-(3-azido-4-methoxy-phenyl)methanone

YTFPVGLVSMVYBP-UHFFFAOYSA-N

Microorganism:

Yes

IUPAC name

bis(3-azido-4-methoxyphenyl)methanone

SMILES

COC1=C(C=C(C=C1)C(=O)C2=CC(=C(C=C2)OC)N=[N+]=[N-])N=[N+]=[N-]

Inchi

InChI=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

Formula

C₁₅H₁₂N₆O₃

PubChem ID

533554

Molweight

324.29

LogP

5.1

Atoms

Bonds

H-bond Acceptor

H-bond Donor

Chemical Classification

aromatic compounds aromatic ketones azides benzenoids ethers ketones nitrogen compounds

mVOC Specific Details

Species emitting the compound

Kingdom	Species	Biological Function	Origin/Habitat	Reference
	Pectobacterium Carotovorum			Kate et al. 2023

Method

Kingdom	Species	Growth Medium	Applied Method	Verification
	Pectobacterium Carotovorum	inoculated potato samples	GC-MS	no

(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

SMILES

CC1CC(=CC2=CC=C(C=C2)N=[N+]=[N-])C(=O)C(=CC3=CC=C(C=C3)N=[N+]=[N-])C1

Inchi

InChI=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+

Formula

C₂₁H₁₈N₆O

PubChem ID

5466536

Molweight

370.4

LogP

7.2

Atoms

Bonds

H-bond Acceptor

H-bond Donor

Chemical Classification

aromatic compounds azides benzenoids ketones nitrogen compounds

mVOC Specific Details

Species emitting the compound

Kingdom	Species	Biological Function	Origin/Habitat	Reference
	Aspergillus Flavus			Kate et al. 2023
	Pectobacterium Carotovorum			Kate et al. 2023

Method

Kingdom	Species	Growth Medium	Applied Method	Verification
	Aspergillus Flavus	inoculated potato samples	GC-MS	no
	Pectobacterium Carotovorum	inoculated potato samples	GC-MS	no

[(E)-1-[1-[(E)-N-(carbamoylamino)-C-methylcarbonimidoyl]cyclopropyl]ethylideneamino]urea

Compound Details

Synonymous names

1,1'-(1,1'-Cyclopropylidenediethylidene)disemicarbazide

HMFLJPJQYZSYKO-BYDSPXIWSA-N

Microorganism:

Yes

IUPAC name

[(E)-1-[1-[(E)-N-(carbamoylamino)-C-methylcarbonimidoyl]cyclopropyl]ethylideneamino]urea

SMILES

CC(=NNC(=O)N)C1(CC1)C(=NNC(=O)N)C

Inchi

InChI=1S/C9H16N6O2/c1-5(12-14-7(10)16)9(3-4-9)6(2)13-15-8(11)17/h3-4H2,1-2H3,(H3,10,14,16)(H3,11,15,17)/b12-5+,13-6+

Formula

C₉H₁₆N₆O₂

PubChem ID

9602844

Molweight

240.26

LogP

-1.4

Atoms

Bonds

H-bond Acceptor

H-bond Donor

Chemical Classification

carbazides nitrogen compounds

mVOC Specific Details

Species emitting the compound

Kingdom	Species	Biological Function	Origin/Habitat	Reference
Eukaryota	Saccharomyces Cerevisiae	NA	NA	Harris et al. 2021

Method

Kingdom	Species	Growth Medium	Applied Method	Verification
Eukaryota	Saccharomyces Cerevisiae	malt extract broth	HS-SPME with GC-MS	no

Results for: chemical Classification: azides

Azidomethylbenzene

Compound Details

mVOC Specific Details

1,3-diaminourea

Compound Details

mVOC Specific Details

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

Compound Details

mVOC Specific Details

3-azidoprop-1-ene

Compound Details

mVOC Specific Details

Bis(3-azido-4-methoxyphenyl)methanone

Compound Details

mVOC Specific Details

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

Compound Details

mVOC Specific Details

[(E)-1-[1-[(E)-N-(carbamoylamino)-C-methylcarbonimidoyl]cyclopropyl]ethylideneamino]urea

Compound Details

mVOC Specific Details

Results for:
chemical Classification: azides