Results for:
chemical Classification: hydrazines

N-(propan-2-ylideneamino)methanamine

Compound Details

Synonymous names
2-Propanone, methylhydrazone
N-(propan-2-ylideneamino)methanamine
Acetone methylhydrazone
5771-02-8
1-methyl-2-(propan-2-ylidene)hydrazine
Acetone N-methylhydrazone
METHYLHYDRAZONE ACETONE
DTXSID20206421
NSC64710
NSC 64710
NSC-64710
NSC166797
1-methyl-2-(2-propylidene)hydrazine
NSC 166797
NSC-166797
Microorganism:

Yes

IUPAC nameN-(propan-2-ylideneamino)methanamine
SMILESCC(=NNC)C
InchiInChI=1S/C4H10N2/c1-4(2)6-5-3/h5H,1-3H3
FormulaC4H10N2
PubChem ID79840
Molweight86.14
LogP0.5
Atoms6
Bonds1
H-bond Acceptor2
H-bond Donor1
Chemical Classificationhydrazines nitrogen compounds

mVOC Specific Details

Massbank-Links

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaAspergillus NigerNANACosta et al. 2016
EukaryotaCandida AlbicansNANACosta et al. 2016
EukaryotaPenicillium ChrysogenumNANACosta et al. 2016
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaAspergillus NigerYeast Glucose ChloramphenicolSPME/GCxGC-MSno
EukaryotaCandida AlbicansYeast Glucose ChloramphenicolSPME/GCxGC-MSno
EukaryotaPenicillium ChrysogenumYeast Glucose ChloramphenicolSPME/GCxGC-MSno


Furan-2-carbohydrazide

Compound Details

Synonymous names
furan-2-carbohydrazide
3326-71-4
2-Furoic acid hydrazide
2-Furoic hydrazide
2-Furohydrazide
Furoylhydrazide
2-Furoylhydrazine
2-Furancarbohydrazide
2-Furoylhydrazide
2-Furancarboxylic acid, hydrazide
Furoic acid, hydrazide
2-Furylcarbonylhydrazide
2-furancarboxylic acid hydrazide
2-Furancarbohydrazonic acid
2-FUROIC ACID, HYDRAZIDE
Pyromucic acid hydrazide
2-Furancarbonyl hydrazide
2-Furylcarboxylic acid hydrazide
MFCD00003235
Furan-2-carboxylic acid hydrazide
NSC 11957
NSC 35574
WLN: T5OJ BVMZ
NSC11957
NSC35574
Furancarboxylic acid, hydrazide
2-Furoicacidhydrazide
EINECS 222-046-2
BRN 0114435
AI3-62534
2-furanhydrazide
2-Furoichydrazide
2-furanoic hydrazide
furan 2-carbohydrazide
2-Furoic hydrazide, 98%
5-18-06-00125 (Beilstein Handbook Reference)
SCHEMBL140989
CHEMBL340492
DTXSID10186900
HMS1775C18
CS-M1764
NSC-11957
NSC-35574
STK121925
AKOS000194881
AM10044
MCULE-6130017029
AS-57679
SY048471
DB-048376
DB-293084
F1015
NS00029450
2-Furoic hydrazide, purum, >=97.0% (NT)
EN300-17784
F10405
A821702
AN-068/40170015
J-019120
J-521392
Z57036326
F3145-4915
InChI=1/C5H6N2O2/c6-7-5(8)4-2-1-3-9-4/h1-3H,6H2,(H,7,8
Microorganism:

Yes

IUPAC namefuran-2-carbohydrazide
SMILESC1=COC(=C1)C(=O)NN
InchiInChI=1S/C5H6N2O2/c6-7-5(8)4-2-1-3-9-4/h1-3H,6H2,(H,7,8)
FormulaC5H6N2O2
PubChem ID18731
Molweight126.11
LogP-0.5
Atoms9
Bonds1
H-bond Acceptor3
H-bond Donor2
Chemical Classificationhydrazines ethers furan derivatives heterocyclic compounds nitrogen compounds
Supernatural-IDSN0348234

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaMetschnikowia HawaiiensisNANALjunggren et al. 2019
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaMetschnikowia Hawaiiensisliquid YPD mediumGC-MSno


4-methoxybenzohydrazide

Mass-Spectra

Compound Details

Synonymous names
4-Methoxybenzhydrazide
4-Methoxybenzohydrazide
3290-99-1
p-Anisic hydrazide
p-Anisoylhydrazine
4-Methoxybenzoic acid hydrazide
Anisic hydrazide
4-Methoxybenzoylhydrazine
Anisoylhydrazine
p-Anisic acid, hydrazide
Anisic acid hydrazide
(p-Methoxybenzoyl)hydrazine
Benzoic acid, 4-methoxy-, hydrazide
4-Methoxybenzene-1-carbohydrazide
p-Methoxybenzoic acid hydrazide
p-Methoxybenzoic hydrazide
(4-Methoxybenzoyl)hydrazide
p-Methoxy benzhydrazide
Hydrazine, 4-methoxybenzoyl-
4-Methoxybenzoyl hydrazide
p-Anisohydrazide
(4-Methoxybenzoyl)hydrazine
Benzoic acid, p-methoxy-, hydrazide
NSC 76223
p-methoxybenzhydrazide
4-methoxy benzhydrazide
p-Methoxybenzoyl hydrazide
CHEMBL1588015
MFCD00017073
NSC-76223
33BK77102I
p-Anisic acid hydrazide
p-methoxy benzohydrazide
EINECS 221-952-5
4-Methoxybenzoic hydrazide
anisohydrazide
BRN 0389017
UNII-33BK77102I
p-methoxybenzohydrazide
4MeOPhCON2
4-methoxy-benzohydrazide
P-ANISOYLHYDRAZIDE
4-Methoxybenzohydrazide #
WLN: ZMVR DO1
Oprea1_578754
Oprea1_834050
303084-44-8
4-10-00-00454 (Beilstein Handbook Reference)
MLS000833598
4-Methoxybenzhydrazide, 97%
SCHEMBL407188
METHOXYBENZHYDRAZIDE, 4-
4-methoxy-benzoic acid hydrazide
4-Methoxybenzoic acid, hydrazide
DTXSID60186556
HMS2804K19
NSC76223
STR02684
BBL005388
BDBM50340089
STK089128
AKOS000194883
MCULE-8901256628
NCGC00246653-01
SMR000457119
SY005826
DB-013162
AM20040183
CS-0116725
M1770
NS00029380
4-methoxybenzohydrazide;4-Methoxybenzhydrazide
EN300-18129
I11428
A821514
W-106806
Q27256258
Z57199662
F1335-0033
Microorganism:

Yes

IUPAC name4-methoxybenzohydrazide
SMILESCOC1=CC=C(C=C1)C(=O)NN
InchiInChI=1S/C8H10N2O2/c1-12-7-4-2-6(3-5-7)8(11)10-9/h2-5H,9H2,1H3,(H,10,11)
FormulaC8H10N2O2
PubChem ID76792
Molweight166.18
LogP0.2
Atoms12
Bonds2
H-bond Acceptor3
H-bond Donor2
Chemical Classificationhydrazines benzenoids ethers aromatic compounds nitrogen compounds
Supernatural-IDSN0323114

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaMycobacterium Bovisclinical isolate,abscess,bladder cancerMellors et al. 2017
ProkaryotaMycobacterium Intracellulareclinical isolate,sputum,AIDS patientMellors et al. 2017
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaMycobacterium Bovis7H9 broth, Tween 80, glycerolTenaxGC,Chromosorb,HS-SPME, GC-MSno
ProkaryotaMycobacterium Intracellulare7H9 broth, Tween 80, glycerolTenaxGC,Chromosorb,HS-SPME, GC-MSno


1-methyl-1-phenylhydrazine

Compound Details

Synonymous names
1-Methyl-1-phenylhydrazine
618-40-6
1-Methylphenylhydrazine
N-Methyl-N-phenylhydrazine
Hydrazine, 1-methyl-1-phenyl-
N-Phenyl-N-methylhydrazine
1-methyl-1-phenyl-hydrazine
.alpha.-Methyl-.alpha.-phenylhydrazine
YHB9CZB63U
N-methyl-N-phenyl-hydrazine
MFCD00007627
NSC-525518
Hydrazine, methylphenyl-
alpha-Methyl-alpha-phenylhydrazine
EINECS 210-547-9
UNII-YHB9CZB63U
NSC 525518
methylphenylhydrazine
NSC525518
methyl phenylhydrazine
n-methylphenylhydrazine
SCHEMBL788
1-methyl 1-phenylhydrazine
1-phenyl-1-methylhydrazine
1-methyl-1-phenyl hydrazine
.alpha.-Methylphenylhydrazine
DTXSID2060678
HMS1761M15
1-Methyl-1-phenylhydrazine, 97%
AMY22640
618-40-6 pound OIAe pound(c)
BBL100336
STL554118
AKOS001098542
FS-4236
MCULE-1026323460
s11053
J29.560D
SY049215
A8562
M0399
NS00034808
EN300-18464
J-505003
Q27294527
Z57985384
InChI=1/C7H10N2/c1-9(8)7-5-3-2-4-6-7/h2-6H,8H2,1H
Microorganism:

Yes

IUPAC name1-methyl-1-phenylhydrazine
SMILESCN(C1=CC=CC=C1)N
InchiInChI=1S/C7H10N2/c1-9(8)7-5-3-2-4-6-7/h2-6H,8H2,1H3
FormulaC7H10N2
PubChem ID36299
Molweight122.17
LogP1.6
Atoms9
Bonds1
H-bond Acceptor2
H-bond Donor1
Chemical Classificationamines hydrazines heterocyclic compounds nitrogen compounds

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaSaccharomyces CerevisiaeNANAHarris et al. 2021
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaSaccharomyces Cerevisiaemalt extract brothHS-SPME with GC-MSno


3-aminobenzohydrazide

Compound Details

Synonymous names
3-Aminobenzhydrazide
14062-34-1
3-Aminobenzohydrazide
3-Aminobenzoyl hydrazine
Benzoic acid, 3-amino-, hydrazide
m-Aminobenzhydrazide
m-Amino benzhydrazide
m-Aminobenzoic acid hydrazide
3-aminobenzoic acid hydrazide
459AL52KFJ
NSC-28878
m-Aminobenzohydrazide
3-Amino-benzoic acid hydrazide
C7-H9-N3-O
EINECS 237-907-8
3-Aminobenzohydrazide #
UNII-459AL52KFJ
3-AMINOBENZOYLHYDRAZIDE
3-AMINOBENZOYLHYDRAZINE
SCHEMBL294944
3-Aminobenzoic acid, hydrazide
M-AMINOBENZOIC HYDRAZIDE
CHEMBL125641
DTXSID4074516
NSC28878
MFCD00017067
NSC 28878
AKOS008966956
MCULE-3299646715
AS-61578
DB-042526
CS-0206379
NS00024558
EN300-17375
E85335
Z56922179
Microorganism:

Yes

IUPAC name3-aminobenzohydrazide
SMILESC1=CC(=CC(=C1)N)C(=O)NN
InchiInChI=1S/C7H9N3O/c8-6-3-1-2-5(4-6)7(11)10-9/h1-4H,8-9H2,(H,10,11)
FormulaC7H9N3O
PubChem ID84178
Molweight151.17
LogP-0.9
Atoms11
Bonds1
H-bond Acceptor3
H-bond Donor3
Chemical Classificationbenzenoids aromatic compounds hydrazines nitrogen compounds amides amines
Supernatural-IDSN0173921

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaSaccharomyces CerevisiaeNANAHarris et al. 2021
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaSaccharomyces Cerevisiaemalt extract brothHS-SPME with GC-MSno


N-[(E)-(4-nitrophenyl)methylideneamino]benzamide

Compound Details

Synonymous names
N'-(4-Nitrobenzylidene)benzohydrazide
N'-[(E)-(4-Nitrophenyl)methylidene]benzohydrazide
PhCON2 4NO2PhCH
Benzoic acid, (4-nitrobenzylidene)hydrazide
N-[(E)-(4-nitrophenyl)methylideneamino]benzamide
MVQGNPRBTFWEMO-XNTDXEJSSA-N
BDBM192660
STK364451
AKOS000612303
MCULE-5950867660
Benzoic acid, (4-nitrophenyl)-methylenehydrozide
N-[(E)-(4-nitrophenyl)methyleneamino]benzamide
A819418
N’-(4-nitrophenylmethylene)benzohydrazide (1k)
N'-[(E)-(4-Nitrophenyl)methylidene]benzohydrazide #
Microorganism:

Yes

IUPAC nameN-[(E)-(4-nitrophenyl)methylideneamino]benzamide
SMILESC1=CC=C(C=C1)C(=O)NN=CC2=CC=C(C=C2)[N+](=O)[O-]
InchiInChI=1S/C14H11N3O3/c18-14(12-4-2-1-3-5-12)16-15-10-11-6-8-13(9-7-11)17(19)20/h1-10H,(H,16,18)/b15-10+
FormulaC14H11N3O3
PubChem ID6861632
Molweight269.25
LogP2.4
Atoms20
Bonds3
H-bond Acceptor4
H-bond Donor1
Chemical Classificationbenzenoids nitro compounds aromatic compounds nitrogen compounds amides hydrazines

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaSaccharomyces CerevisiaeNANAHarris et al. 2021
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaSaccharomyces Cerevisiaemalt extract brothHS-SPME with GC-MSno