Results for:
chemical Classification: carbamates

(3-carbamoyloxy-2-phenylpropyl) Carbamate

Compound Details

Synonymous names
felbamate
25451-15-4
Felbatol
2-Phenylpropane-1,3-diyl dicarbamate
2-Phenyl-1,3-propanediol dicarbamate
Felbamyl
Taloxa
Felbamatum
Felbamato
W-554
1,3-Propanediol, 2-phenyl-, dicarbamate
Felbamatum [Latin]
ADD-03055
carbamic acid 2-phenyltrimethylene ester
W 554
CHEBI:4995
Carbamic acid, 2-phenyltrimethylene ester
EINECS 247-001-4
UNII-X72RBB02N8
NSC-759866
BRN 3345236
X72RBB02N8
DTXSID9023041
HSDB 7525
3-(carbamoyloxy)-2-phenylpropyl carbamate
(3-carbamoyloxy-1,1,3,3-tetradeuterio-2-phenylpropyl) carbamate
2-Phenyl-1,3-propanediol 1,3-dicarbamate
MLS000028465
DTXCID903041
4-06-00-05993 (Beilstein Handbook Reference)
Carbamic acid 3-carbamoyloxy-2-phenyl-propyl ester
Felbamatum (Latin)
MFCD00865296
NSC 759866
NCGC00015429-08
W-554;ADD-03055
Felbamato [Spanish]
SMR000058448
FELBAMATE (MART.)
FELBAMATE [MART.]
FELBAMATE (USP-RS)
FELBAMATE [USP-RS]
Felbamate [USAN:INN]
FELBAMATE (USP MONOGRAPH)
FELBAMATE [USP MONOGRAPH]
(3-carbamoyloxy-2-phenylpropyl) carbamate
Felbatol (TN)
CAS-25451-15-4
SR-01000000089
ADD 03055
2 Phenyl 1,3 propanediol dicarbamate
Felbamate (USPINN)
Tocris-0869
FELBAMATE [INN]
FELBAMATE [MI]
FELBAMATE [HSDB]
FELBAMATE [USAN]
Opera_ID_1738
Prestwick0_000919
FELBAMATE [VANDF]
Lopac-F-0778
Biomol-NT_000203
F 0778
FELBAMATE [WHO-DD]
CHEMBL1094
Lopac0_000524
SCHEMBL34947
MLS001077299
BIDD:GT0463
BPBio1_001258
GTPL5473
FELBAMATE [ORANGE BOOK]
EX-A591
N03AX10
HMS2093P19
HMS2234H06
HMS3261J09
HMS3266L12
HMS3370I06
HMS3411P21
HMS3657I11
HMS3675P21
HMS3715D20
HMS3884E11
Pharmakon1600-01505600
BCP27941
HY-B0184
Tox21_110145
Tox21_302368
Tox21_500524
BDBM50088430
NSC759866
s1330
AKOS015895100
Tox21_110145_1
AC-8197
CCG-204614
CS-2068
DB00949
KS-1171
LP00524
MCULE-2661497722
SDCCGSBI-0050507.P003
NCGC00015429-01
NCGC00015429-02
NCGC00015429-03
NCGC00015429-04
NCGC00015429-05
NCGC00015429-06
NCGC00015429-07
NCGC00015429-09
NCGC00015429-10
NCGC00015429-11
NCGC00015429-14
NCGC00015429-24
NCGC00023092-02
NCGC00023092-04
NCGC00023092-05
NCGC00023092-06
NCGC00255275-01
NCGC00261209-01
SBI-0050507.P002
DB-046702
AE2 - Newer Anti-epileptic drug mixtures 2
EU-0100524
NS00010360
SW197633-2
(3-aminocarbonyloxy-2-phenyl-propyl) carbamate
C07501
D00536
EN300-119542
AB00382985-18
AB00382985_19
A817858
Q421301
carbamic acid (3-carbamoyloxy-2-phenylpropyl) ester
Q-100326
SR-01000000089-2
SR-01000000089-4
SR-01000000089-7
BRD-K99107520-001-01-9
BRD-K99107520-001-09-2
BRD-K99107520-001-18-3
Z1521554005
Felbamate, United States Pharmacopeia (USP) Reference Standard
Microorganism:

Yes

IUPAC name(3-carbamoyloxy-2-phenylpropyl) carbamate
SMILESC1=CC=C(C=C1)C(COC(=O)N)COC(=O)N
InchiInChI=1S/C11H14N2O4/c12-10(14)16-6-9(7-17-11(13)15)8-4-2-1-3-5-8/h1-5,9H,6-7H2,(H2,12,14)(H2,13,15)
FormulaC11H14N2O4
PubChem ID3331
Molweight238.24
LogP0.6
Atoms17
Bonds7
H-bond Acceptor4
H-bond Donor2
Chemical Classificationaromatic compounds carbamates nitrogen compounds benzenoids
CHEBI-ID4995
Supernatural-IDSN0412584

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


Phenyl N-methylcarbamate

Compound Details

Synonymous names
PHENYL METHYLCARBAMATE
1943-79-9
Phenyl N-methylcarbamate
Methylcarbamic acid phenyl ester
N-Methylphenylcarbamate
Phenmec
Phenyl monomethylcarbamate
Carbamic acid, methyl-, phenyl ester
Phenol, methylcarbamate
Phenyl-N-methylcarbamate
Carbamic acid,N-methyl-, phenyl ester
DRC 3345
Methyl carbamic acid phenyl ester
methyl-carbamic acid phenyl ester
MFCD01738783
19U7Y0R088
NSC-128138
Carbamic acid, N-methyl-, phenyl ester
CCRIS 1835
HSDB 2598
NSC 128138
BRN 2045075
AI3-33080
UNII-19U7Y0R088
Phenylmethylcarbamate
phenyl(methyl)carbamate
WLN: 1MVOR
SCHEMBL78497
4-06-00-00630 (Beilstein Handbook Reference)
CHEMBL2046815
DTXSID1073282
BDBM50004688
NSC128138
N-METHYLPHENYLCARBAMATE [HSDB]
AKOS006242248
MS-20800
SY269947
DB-065852
CS-0160301
NS00125245
C10489
Q27252134
Microorganism:

Yes

IUPAC namephenyl N-methylcarbamate
SMILESCNC(=O)OC1=CC=CC=C1
InchiInChI=1S/C8H9NO2/c1-9-8(10)11-7-5-3-2-4-6-7/h2-6H,1H3,(H,9,10)
FormulaC8H9NO2
PubChem ID16034
Molweight151.16
LogP1.2
Atoms11
Bonds2
H-bond Acceptor2
H-bond Donor1
Chemical Classificationaromatic compounds carbamates nitrogen compounds benzenoids

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaStenotrophomonas Maltophiliaantifungal activity against Colletotrichum nymphaeaeisolated from the healthy strawberry leaf in Kamyaran, Kurdistan provinceAlijani et al. 2020
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaStenotrophomonas MaltophiliaNA mediaGC-MSno


[4-(dimethylamino)-3-methylphenyl] N-methylcarbamate

Compound Details

Synonymous names
AMINOCARB
Matacil
2032-59-9
Aminocarbe
Mitacil
Matacil 180D
Bayer 5080
Bayer 44646
4-(Dimethylamino)-3-methylphenyl methylcarbamate
4-(Dimethylamino)-m-tolyl methylcarbamate
BAY 44646
ENT 25,784
4-Dimethylamino-3-cresyl methylcarbamate
A 363
3-Methyl-4-dimethylaminophenyl methylcarbamate
Phenol, 4-(dimethylamino)-3-methyl-, methylcarbamate (ester)
(4-Dimethylamino-3-methyl-phenyl)N-methyl-carbamate
Carbamic acid, methyl-, 4-(dimethylamino)-m-tolyl ester
4-(Dimethylamino)-3-cresyl methylcarbamate
CHEBI:2653
DTXSID7022172
Carbamic acid, methyl-, 4-(dimethylamino)-3-methylphenyl ester
4-(Dimethylamino)-3-methylphenol methyl carbamate
(4-Dimethylamino-3-methyl-phenyl)N-methyl-carbamat
(4-Dimetilamino-3-metil-fenil)-N-metil-carbammato
4-(dimethylamino)-3-methylphenyl N-methylcarbamate
(4-Dimethylamino-3-methyl-phenyl)N-methyl-carbamaat
N-Methylcarbamate de 4-dimethylamino 3-methyl phenyle
767M03K32Y
Aminocarbe [French]
Caswell No. 360
Aminocarb [BSI:ISO]
Aminocarbe [ISO-French]
HSDB 561
EINECS 217-990-7
EPA Pesticide Chemical Code 044401
4-Dimethylamine m-cresyl methylcarbamate
4-Dimethylamine-m-cresyl methylcarbamate
BRN 2808681
AI3-25784
UNII-767M03K32Y
Methylcarbamic acid 4-(dimethylamino)-m-tolyl ester
[4-(dimethylamino)-3-methylphenyl] N-methylcarbamate
m-Cresol, 4-(dimethylamino)-, methylcarbamate (ester)
4-(Dimethylamino)-3-methylphenol methyl carbamate (ester)
4-(Dimethylamino)-3-methylphenol methylcarbamate (ester)
(4-Dimethylamino-3-methyl-phenyl)N-methyl-carbamaat [Dutch]
(4-Dimethylamino-3-methyl-phenyl)N-methyl-carbamat [German]
(4-Dimetilamino-3-metil-fenil)-N-metil-carbammato [Italian]
AMINOCARB [ISO]
AMINOCARB [MI]
N-Methylcarbamate de 4-dimethylamino 3-methyl phenyle [French]
AMINOCARB [HSDB]
(4-Dimethylamino-3-methylphenyl) N-methylcarbamate
SCHEMBL119059
Carbamic acid, methyl-, 4-dimethylamino-m-tolyl ester
DTXCID302172
CHEMBL1079605
CAA03259
Tox21_301423
Aminocarb 100 microg/mL in Acetonitrile
NCGC00163800-01
NCGC00255150-01
4-Dimethylamino- m-cresyl methylcarbamate
4-(Dimethylamino)-3-tolyl methylcarbamate
CAS-2032-59-9
DB-045174
NS00008504
4-Dimethylamino-3-methylphenyl methylcarbamate
Aminocarb, PESTANAL(R), analytical standard
m-Cresol, 4-(dimethylamino)-, methylcarbamate
3-Methyl-4-(Dimethylamino)phenyl methylcarbamate
J-013217
Q3120938
Phenol, 4-(dimethylamino)-3-methyl-, methylcarbamate
Microorganism:

Yes

IUPAC name[4-(dimethylamino)-3-methylphenyl] N-methylcarbamate
SMILESCC1=C(C=CC(=C1)OC(=O)NC)N(C)C
InchiInChI=1S/C11H16N2O2/c1-8-7-9(15-11(14)12-2)5-6-10(8)13(3)4/h5-7H,1-4H3,(H,12,14)
FormulaC11H16N2O2
PubChem ID16247
Molweight208.26
LogP1.9
Atoms15
Bonds3
H-bond Acceptor3
H-bond Donor1
Chemical Classificationaromatic compounds carbamates nitrogen compounds amines benzenoids
CHEBI-ID2653
Supernatural-IDSN0149424

mVOC Specific Details

Volatilization
Based on an estimated Henry's Law constant of 5.636X10-10 atm-cu m/mole(1), the volatilization half-life of aminocarb from a 1 m deep model river flowing at a current speed of 1 m/sec and a wind speed of 3 m/sec would be hundreds of years(2,SRC). Therefore, volatilization of aminocarb from water may not be important(SRC).
Soil Adsorption
Based on regression equations(3) and the water solubility of 915 mg/l(1) and a log Kow value of 1.734(2), the estimated log Koc for aminocarb is in the range 2.01-2.32(SRC). According to a suggested classification scheme(4), this range of log Koc values indicates that aminocarb is moderately to highly mobile in soil(4). Conversely, it would be weakly to moderately sorbed to suspended soils and sediment in water(SRC).
Massbank-Links

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-amino-1,3-oxazolidin-2-one

Compound Details

Synonymous names
3-Amino-2-oxazolidinone
80-65-9
3-Aminooxazolidin-2-one
3-Amino-1,3-oxazolidin-2-one
2-Oxazolidinone, 3-amino-
3-Amino-2-oxazolidone
AOZ
NSC38250
VJ7HE86A15
MFCD00020871
NSC-38250
NSC-111187
NSC-196570
3-Amino-2-oxazolidinone AOZ
NSC 111187
3-Amino-2-oxazolidinone (AOZ)
EINECS 201-299-2
3-amino oxazolidinone
UNII-VJ7HE86A15
3-aminooxazolidin-2-id-4-one
SCHEMBL1163805
DTXSID00229996
CHEBI:173320
BCP32566
3-Amino-1,3-oxazolidin-2-one #
NSC111187
NSC196570
AKOS006228286
1ST4201
CS-W013698
HY-W012982
MCULE-7407834106
s10190
AC-33916
AOZ, VETRANAL(TM), analytical standard
AS-57894
SY038618
NS00015373
EN300-115889
A839960
A936035
F9995-4179
Z1198147716
3-Amino-2-oxazolidinone (AOZ) 100 microg/mL in Acetonitrile
InChI=1/C3H6N2O2/c4-5-1-2-7-3(5)6/h1-2,4H
2-Oxazolidinone, 3-amino-;3-Amino-1,3-oxazolidin-2-one;3-Aminooxazolidin-2-one
Microorganism:

Yes

IUPAC name3-amino-1,3-oxazolidin-2-one
SMILESC1COC(=O)N1N
InchiInChI=1S/C3H6N2O2/c4-5-1-2-7-3(5)6/h1-2,4H2
FormulaC3H6N2O2
PubChem ID65725
Molweight102.09
LogP-0.8
Atoms7
Bonds0
H-bond Acceptor3
H-bond Donor1
Chemical Classificationamides oxazolidinones nitrogen compounds carbamates heterocyclic compounds
CHEBI-ID173320

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaBacillus AcidicelerNAMéndez-Bravo et al. 2018
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaBacillus AcidicelerLB agarSPME / GS-MSno


(2S)-3-(1H-imidazol-5-yl)-2-(phenylmethoxycarbonylamino)propanoic Acid

Compound Details

Synonymous names
Z-His-OH
14997-58-1
N-Cbz-L-histidine
L-Histidine, N-[(phenylmethoxy)carbonyl]-
CBZ-histidine
Nalpha-Cbz-L-histidine
Nalpha-Carbobenzoxy-L-histidine
(2S)-3-(1H-imidazol-5-yl)-2-(phenylmethoxycarbonylamino)propanoic acid
MFCD00065960
N-[(Benzyloxy)carbonyl]-L-histidine
Histidine, N-[(phenylmethoxy)carbonyl]-
(2S)-2-{[(benzyloxy)carbonyl]amino}-3-(1H-imidazol-4-yl)propanoic acid
(s)-2-(((benzyloxy)carbonyl)amino)-3-(1h-imidazol-5-yl)propanoic acid
Cbz-L-histidine
Cbz-His
N-(alpha)-Carbobenzoxy-L-histidine
N-alpha-benzyloxycarbonyl-L-histidine
N|A-Cbz-L-histidine
benzyloxycarbonyl-L-histidine
N-CBZ-L-HISTIDINE-OH
Z-His-OH, 99%
SCHEMBL254638
SCHEMBL9230979
((Benzyloxy)carbonyl)-L-histidine
DTXSID501280353
Nalpha -benzyloxycarbonyl-histidine
AMY31373
(S)-2-(BENZYLOXYCARBONYLAMINO)-3-(1H-IMIDAZOL-4-YL)PROPANOIC ACID
AKOS015909985
AKOS015924085
CS-W013996
FD21657
HY-W013280
MCULE-4620948899
N-[(Phenylmethoxy)carbonyl]-L-histidine
AC-17159
AS-49151
DB-030164
B0265
NS00051681
EN300-121289
M03075
A808989
W-108080
Microorganism:

Yes

IUPAC name(2S)-3-(1H-imidazol-5-yl)-2-(phenylmethoxycarbonylamino)propanoic acid
SMILESC1=CC=C(C=C1)COC(=O)NC(CC2=CN=CN2)C(=O)O
InchiInChI=1S/C14H15N3O4/c18-13(19)12(6-11-7-15-9-16-11)17-14(20)21-8-10-4-2-1-3-5-10/h1-5,7,9,12H,6,8H2,(H,15,16)(H,17,20)(H,18,19)/t12-/m0/s1
FormulaC14H15N3O4
PubChem ID736313
Molweight289.29
LogP1.2
Atoms21
Bonds7
H-bond Acceptor5
H-bond Donor3
Chemical Classificationacids imidazoles benzenoids carbamates carboxylic acids heterocyclic compounds aromatic compounds nitrogen compounds organic acids

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


Butyl 2-(2-methylpropoxycarbonylamino)propanoate

Compound Details

Synonymous names
l-Alanine, N-isobutoxycarbonyl-, butyl ester
RNKTVMOYIULYFP-UHFFFAOYSA-N
Microorganism:

Yes

IUPAC namebutyl 2-(2-methylpropoxycarbonylamino)propanoate
SMILESCCCCOC(=O)C(C)NC(=O)OCC(C)C
InchiInChI=1S/C12H23NO4/c1-5-6-7-16-11(14)10(4)13-12(15)17-8-9(2)3/h9-10H,5-8H2,1-4H3,(H,13,15)
FormulaC12H23NO4
PubChem ID6423190
Molweight245.32
LogP2.8
Atoms17
Bonds9
H-bond Acceptor4
H-bond Donor1
Chemical Classificationcarbamates nitrogen compounds esters

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


Heptyl 6-(butoxycarbonylamino)hexanoate

Compound Details

Synonymous names
UOEXELOVYXULHX-UHFFFAOYSA-N
6-Aminocaproic acid, n-butoxycarbonyl-, heptyl ester
Microorganism:

No

IUPAC nameheptyl 6-(butoxycarbonylamino)hexanoate
SMILESCCCCCCCOC(=O)CCCCCNC(=O)OCCCC
InchiInChI=1S/C18H35NO4/c1-3-5-7-8-12-16-22-17(20)13-10-9-11-14-19-18(21)23-15-6-4-2/h3-16H2,1-2H3,(H,19,21)
FormulaC18H35NO4
PubChem ID91736380
Molweight329.5
LogP5
Atoms23
Bonds17
H-bond Acceptor4
H-bond Donor1
Chemical Classificationcarbamates esters nitrogen compounds

mVOC Specific Details


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


Nonyl 4-methylsulfanyl-2-(prop-2-ynoxycarbonylamino)butanoate

Compound Details

Synonymous names
DCKZYEHULVPSPD-UHFFFAOYSA-N
l-Methionine, n-propargyloxycarbonyl-, nonyl ester
Microorganism:

No

IUPAC namenonyl 4-methylsulfanyl-2-(prop-2-ynoxycarbonylamino)butanoate
SMILESCCCCCCCCCOC(=O)C(CCSC)NC(=O)OCC#C
InchiInChI=1S/C18H31NO4S/c1-4-6-7-8-9-10-11-14-22-17(20)16(12-15-24-3)19-18(21)23-13-5-2/h2,16H,4,6-15H2,1,3H3,(H,19,21)
FormulaC18H31NO4S
PubChem ID91740822
Molweight357.5
LogP5
Atoms24
Bonds16
H-bond Acceptor5
H-bond Donor1
Chemical Classificationcarbamates esters nitrogen compounds sulfur compounds thioethers

mVOC Specific Details


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