Results for:
Species: Lentinellus cochleatus

Methyl 4-methoxybenzoate

Mass-Spectra

Compound Details

Synonymous names
DDIZAANNODHTRB-UHFFFAOYSA-N
methyl4-methoxybenzoate
Methyl p-methoxybenzoate
Methyl anisate
METHYL 4-METHOXYBENZOATE
4-methoxy methylbenzoate
METHYL PARA-ANISATE
Methyl p-anisate
methyl P-methoxy benzoate
Methyl-p-anisate
Methyl-p-Methoxy Benzoate
p-Methoxybenzoic acid methyl ester
ANISIC ACID METHYL ESTER
4-Methoxybenzoic acid methyl
4-(Methoxycarbonyl)anisole
Methyl 4-Anisate
AC1L1R4M
Methyl ester of p-Methoxybenzoic acid
4-Methoxybenzoic acid methyl ester
p-Anisic acid methyl ester
KSC119E6R
NSC7324
ACMC-209ajc
ZINC87933
4-methoxy-benzoic acid methyl ester
SCHEMBL231243
AS02499
ARONIS011593
RP22885
p-Anisic acid, methyl ester
2MFL7873W9
FEMA 2679
bmse010016
AN-9346
NSC 7324
ZB003141
DTXSID7047645
NSC-7324
OR011231
OR209324
SY003911
STK041805
AC-7084
CHEMBL1762668
SBB058204
LS-2900
M-5922
CHEBI:86903
UNII-2MFL7873W9
WLN: 1OVR DO1
SC-24120
KB-54413
AJ-10791
BR-46595
ST2413419
AK-46595
CJ-00703
Methyl p-anisate, 99%
DSSTox_GSID_47645
ANW-17926
DSSTox_CID_27645
RARECHEM AL BF 0083
MFCD00008437
ZINC00087933
BDBM50340087
DSSTox_RID_82472
TR-003554
DB-012814
AM20050128
RTR-003554
ST45048310
AI3-00229
AKOS000501135
I01-8152
W-108443
BRN 2208571
Benzoic acid, p-methoxy-, methyl ester
FT-0628647
FEMA No. 2679
LABOTEST-BB LT00782008
Tox21_302682
Methyl p-anisate, >=99%, FG
F1335-0002
Benzoic acid, 4-methoxy-, methyl ester
121-98-2
MCULE-7764530900
Methyl p-anisate, >=99% (capillary GC)
NCGC00256751-01
CAS-121-98-2
EINECS 204-513-2
MolPort-000-690-489
AQ-917/40232598
InChI=1/C9H10O3/c1-11-8-5-3-7(4-6-8)9(10)12-2/h3-6H,1-2H
Microorganism:

Yes

IUPAC namemethyl 4-methoxybenzoate
SMILESCOC1=CC=C(C=C1)C(=O)OC
InchiInChI=1S/C9H10O3/c1-11-8-5-3-7(4-6-8)9(10)12-2/h3-6H,1-2H3
FormulaC9H10O3
PubChem ID8499
Molweight166.176
LogP1.82
Atoms22
Bonds22
H-bond Acceptor2
H-bond Donor0
Chemical ClassificationBenzenoids Esters Ethers

Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
BacteriaChondromyces Crocatusn/aRespiratory clinical isolates (Canterbury Health Laboratories, Christchurch, New Zealand)Schulz and Dickschat, 2007
BacteriaChondromyces Crocatus Cm C2n/aRespiratory clinical isolates (Canterbury Health Laboratories, Christchurch, New Zealand)Dickschat et al., 2005_6
BacteriaChondromyces Crocatus Cm C5n/aDickschat et al., 2005_6
BacteriaMycobacterium Tuberculosisn/aRespiratory clinical isolates (Canterbury Health Laboratories, Christchurch, New Zealand)Syhre et al., 2008
FungiPiptoporus BetulinusnaSachsenwald near HamburgRösecke et al., 2000
FungiTrametes Suaveolensnanear Zachersmühle, Göppingen, southern GermanyRösecke et al., 2000
FungiLentinellus CochleatusRapior et al. 2002
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
BacteriaChondromyces CrocatusLoewenstein-Jensen/Glycerol, sheep blood agar and BacT/Alerts MPSolid phase micro-extraction (SPME), GC/MS-MS
BacteriaChondromyces Crocatus Cm C2Loewenstein-Jensen/Glycerol, sheep blood agar and BacT/Alerts MPSolid phase micro-extraction (SPME), GC/MS-MS
BacteriaChondromyces Crocatus Cm C5Loewenstein-Jensen/Glycerol, sheep blood agar and BacT/Alerts MPSolid phase micro-extraction (SPME), GC/MS-MS
BacteriaMycobacterium TuberculosisLoewenstein-Jensen/Glycerol, sheep blood agar and BacT/Alerts MPSolid phase micro-extraction (SPME), GC/MS-MS
FungiPiptoporus BetulinusnaGC/MSNo
FungiTrametes SuaveolensnaGC/MSNo
FungiLentinellus Cochleatushydro-destillation, solvent extraction, GC-MSno


4-methoxybenzaldehyde

Mass-Spectra

Compound Details

Synonymous names
p-Methoxybenzylidenemalonitrile
Methoxybenzaldehyde
paraanisaldehyde
para-methoxybenzaldehyde
Anisaldehyde
Anisaldehyde solution
p-Methoxybenzafdehyde
p-Methoxybenzaldehyde
anisaldehyd
4-methoxylbenzaldehyde
Aubepine
Crategine
para-anisaldehyde
ZRSNZINYAWTAHE-UHFFFAOYSA-N
4-Methoxybenzaldehyde
4-Methoxybenzaldhyde
Anisic aldehyde
Obepin
p-Formylanisole
4-methoxybenzahyde
Anis aldehyde
NATURAL ANISIC ALDEHYDE
P-ANISALDEHYDE
p-methoxy benzaldehyde
Methoxybenzaldehyde (Related)
p-Anisaldehyde, primary pharmaceutical reference standard
4-Anisaldehyde
4-methoxy benzaldehyde
4-Methoxy-benzaldehyde
AC1Q4CCF
p-Anisaldehyde, analytical standard
p-Anisic aldehyde
ACMC-1BAZN
p-anis aldehyde
p-Methoxy Benzaldehyde, Natural
p-Methoxybenzaldehyde (natural)
4-(methyloxy)benzaldehyde
Anisaldehyde (para)
Formylanisole, p-
p-Anisic aldehyde; p-Methoxybenzaldehyde; Anisaldehyde
SCHEMBL1100
AC1L1L81
anisic aldehyde (natural)
I922
KSC174M6D
p-Anisaldehyde (4-Methoxybenzaldehyde)
EBD1062
NSC5590
PubChem22535
A0480
CCRIS 821
CTK0H4661
AS02988
Benzaldehyde, 4-methoxy-
CHEMBL161598
p-Anisaldehyde, 98%
RP20260
9PA5V6656V
bmse010130
C10761
HMS3039F08
HSDB 2641
WLN: VHR DO1
ZINC157146
BBL027436
DTXSID2026997
Jsp001555
LS-2093
NSC 5590
NSC-5590
OR034277
OR156303
OR250016
OR250017
OR275512
SBB040224
ZB006571
A805017
DSSTox_CID_6997
M-6033
p-Anisaldehyde, certified reference material, TraceCERT(R)
p-Anisaldehyde, United States Pharmacopeia (USP) Reference Standard
Para Anisic Aldehyde, 4-Methoxy Benzaldehyde.
UNII-9PA5V6656V
AC-10379
AJ-14902
AK-72956
AN-22903
ANW-18100
BR-72956
Caswell No. 051E
CJ-01596
DSSTox_GSID_26997
LS-20018
SC-26765
ST2411506
TRA0080347
BB_NC-2206
BDBM50139370
DSSTox_RID_78277
MFCD00003385
ZINC00157146
AI3-00223
CCG-214805
DB-012818
KB-115367
KB-193002
METHYL, (4-METHOXYPHENYL)OXO-
RTR-003659
ST50213373
TR-003659
AKOS000118814
I01-0482
I01-8766
Q-100105
BRN 0471382
FEMA No. 2670
FT-0617622
MLS002152921
SMR001224521
Tox21_201943
Tox21_303331
123-11-5
4-Methoxybenzaldehyde, 98% 50g
BENZALDEHYDE,4-METHOXY MFC8 H8 O2
F2190-0575
p-Anisaldehyde, for synthesis, 98.0%
p-Anisaldehyde, natural, 98%, FG
MCULE-9537754812
NCGC00090807-01
NCGC00090807-02
NCGC00257076-01
NCGC00259492-01
CAS-123-11-5
EINECS 204-602-6
EINECS 256-891-3
26249-15-0
68894-36-0
EC 204-602-6
721942-53-6
MolPort-000-871-198
p-Anisaldehyde, >=97.5%, FCC, FG
29578-EP2284160A1
29578-EP2292628A2
29578-EP2305695A2
29578-EP2305696A2
29578-EP2305697A2
29578-EP2305698A2
29578-EP2308838A1
29578-EP2311825A1
29578-EP2311842A2
79582-EP2287153A1
79582-EP2292628A2
79582-EP2298755A1
79582-EP2305695A2
79582-EP2305696A2
79582-EP2305697A2
79582-EP2305698A2
79582-EP2374783A1
79582-EP2377841A1
4-08-00-00252 (Beilstein Handbook Reference)
InChI=1/C8H8O2/c1-10-8-4-2-7(6-9)3-5-8/h2-6H,1H
Microorganism:

Yes

IUPAC name4-methoxybenzaldehyde
SMILESCOC1=CC=C(C=C1)C=O
InchiInChI=1S/C8H8O2/c1-10-8-4-2-7(6-9)3-5-8/h2-6H,1H3
FormulaC8H8O2
PubChem ID31244
Molweight136.15
LogP1.53
Atoms18
Bonds18
H-bond Acceptor2
H-bond Donor0
Chemical ClassificationAldehydes Benzenoids Ethers

mVOC Specific Details

Vapor Pressure
PressureReference
1 MM HG @ 73 DEG CClayton, G. D. and F. E. Clayton (eds.). Patty's Industrial Hygiene and Toxicology: Volume 2A, 2B, 2C: Toxicology. 3rd ed. New York: John Wiley Sons, 1981-1982., p. 2663
MS-Links
1D-NMR-Links

Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
FungiDaedalea Juniperinan/aStotzky and Schenk, 1976
Fungi Polyporus BenzoinusBirkinshaw et al 1952
Fungi Trametes SuaveolensBirkinshaw et al. 1945
Fungi Bjerkandera AdustaSpinnler at al. 1998
FungiClitocybe OdoraRapior et al. 2002
FungiLentinellus CochleatusRapior et al. 2002
FungiBjerkandera Adusta CBS 595.78n/aLapadatescu et al., 2000
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
FungiDaedalea Juniperinan/an/a
Fungi Polyporus Benzoinusno
Fungi Trametes Suaveolensno
Fungi Bjerkandera Adustano
FungiClitocybe Odorahydro-destillation, solvent extraction, GC-MSno
FungiLentinellus Cochleatushydro-destillation, solvent extraction, GC-MSno
FungiBjerkandera Adusta CBS 595.78Minimal media plus glucose and L-phenylalanineExtraction with dichloromethane or with ethyl acetate, concentration under N2 stream /GC-MS.