Results for:
chemical Classification: oximes

N-propan-2-ylidenehydroxylamine

Mass-Spectra

Compound Details

Synonymous names
N-isopropylidenehydroxylamine
beta-Isonitrosopropane
Acetoneoxime
N-isopropylidene-hydroxylamine
Acetonoxime
PXAJQJMDEXJWFB-UHFFFAOYSA-N
Acetoxime
propanone oxime
Acetone oxime
ACETONE-OXIME
N-propan-2-ylidenehydroxylamine
.beta.-Isonitrosopropane
Acetone, oxime
Acetoxime >99%
2-Propanone oxime
CCRIS 5
AC1Q2A1Q
AC1Q4SV0
QX74TFD64T
KSC177C7T
Acetone oxime(Di Methyl Ketoxime)
AC1L270Q
propan-2-one oxime
Propane-2-one oxime
Acetoxime; 2-Propanone oxime
ACMC-1C1J8
UNII-QX74TFD64T
NSC7601
2-Propanone, oxime
A0065
CTK0H7179
X9685
N-(propan-2-ylidene)hydroxylamine
LS00155
(CH3)2C=NOH
AM90369
RP18316
C01995
Acetone oxime, 98%
NSC 7601
NSC-7601
AK105880
OR034620
OR211511
DTXSID6020010
MP-2107
LS-2096
Jsp001711
ZINC5442063
A805635
CHEBI:15349
KB-47080
TRA0049718
ST2413699
SC-25907
CJ-12625
AB1004364
ANW-18957
AN-43575
AJ-54116
ZINC05442063
MFCD00002118
AI3-52259
TR-003904
RTR-003904
DB-062562
J-005459
WLN: QNUY1 & 1
S14-1438
AKOS005068118
BRN 1560146
FT-0621800
EN300-31960
127-06-0
MCULE-3243100216
EINECS 204-820-1
Acetone oxime, Vetec(TM) reagent grade, 98%
MolPort-001-779-719
77336-EP2308831A1
77336-EP2301918A1
77336-EP2275407A1
Acetone oxime, purum, >=98.0% (GC)
4-01-00-03202 (Beilstein Handbook Reference)
InChI=1/C3H7NO/c1-3(2)4-5/h5H,1-2H
IUPAC nameN-propan-2-ylidenehydroxylamine
SMILESCC(=NO)C
InchiInChI=1S/C3H7NO/c1-3(2)4-5/h5H,1-2H3
FormulaC3H7NO
PubChem ID67180
Molweight73.095
LogP0.12
Atoms12
Bonds11
H-bond Acceptor2
H-bond Donor1
Chemical Classificationoximes

mVOC Specific Details


Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
BacteriaProteus Penneri YMF3·00016nanaSu et al., 2016
BacteriaProteus Vulgaris Sp.nanaSu et al., 2016
BacteriaPseudochrobactrum Asaccharolyticum YMF3·00201nanaSu et al., 2016
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
BacteriaProteus Penneri YMF3·00016LB mediumSPME-GC/MSNo
BacteriaProteus Vulgaris Sp.LB mediumSPME-GC/MSNo
BacteriaPseudochrobactrum Asaccharolyticum YMF3·00201LB mediumSPME-GC/MSNo


Methyl (Z)-N-hydroxybenzenecarboximidate

Compound Details

Synonymous names
Methyl N-hydroxybenzenecarboximidoate #
HUYDCTLGGLCUTE-HJWRWDBZSA-N
SCHEMBL8530447
Oxime-, methoxy-phenyl-_
IUPAC namemethyl (Z)-N-hydroxybenzenecarboximidate
SMILESCOC(=NO)C1=CC=CC=C1
InchiInChI=1S/C8H9NO2/c1-11-8(9-10)7-5-3-2-4-6-7/h2-6,10H,1H3/b9-8-
FormulaC8H9NO2
PubChem ID9602988
Molweight151.165
LogP1.75
Atoms20
Bonds20
H-bond Acceptor3
H-bond Donor1
Chemical Classificationbenzenoids ethers nitrogen compounds oximes

mVOC Specific Details


Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
BacteriaBacillus Amyloliquefaciens FZB42Agriculture University of Nanjing, ChinaTahir et al. 2025
BacteriaShewanella Algae YM14nasea sediment in east China coastGong et al., 2015
BacteriaPedobacter Sp. V48narhizosphere of Marram grass in sandy dune soils, NetherlandsGarbeva et al., 2014
FungiAscocoryne Sarcoides NRRL 50072n/aMallette et al. 2012
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
BacteriaBacillus Amyloliquefaciens FZB42LBSPME-GC-MSno
BacteriaShewanella Algae YM14NA mediumSPME-GC/MSNo
BacteriaPedobacter Sp. V48sand containing artificial root exudatesGC/MSNo
FungiAscocoryne Sarcoides NRRL 50072Minimal mediumPTR-MS and SPME GC-MS