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> Main
CHEBI:28235 -
p
-methoxybenzaldehyde
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ChEBI Name
p
-methoxybenzaldehyde
ChEBI ID
CHEBI:28235
ChEBI ASCII Name
p-methoxybenzaldehyde
Definition
A member of the class of benzaldehydes consisting of benzaldehyde itself carrying a methoxy substituent at position 4.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:10619, CHEBI:25819
Supplier Information
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Read full article at Wikipedia
Formula
C8H8O2
Net Charge
0
Average Mass
136.148
Monoisotopic Mass
136.05243
InChI
InChI=1S/C8H8O2/c1-10-8-4-2-7(6-9)3-5-8/h2-6H,1H3
InChIKey
ZRSNZINYAWTAHE-UHFFFAOYSA-N
SMILES
C=1(C=CC(C(=O)[H])=CC1)OC
Metabolite of Species
Details
Pseudomonas putida
(NCBI:txid303)
of strain JYR-1 See:
PubMed
Myrrhis odorata
(NCBI:txid40880)
See:
PubMed
Foeniculum vulgare
(NCBI:txid48038)
See:
PubMed
Artemisia dracunculus
(NCBI:txid72341)
See:
PubMed
Homo sapiens
(NCBI:txid9606)
Found in saliva
(UBERON:0001836)
. See:
PubMed
Roles Classification
Biological Role
(s):
human urinary metabolite
Any metabolite (endogenous or exogenous) found in human urine samples.
plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
bacterial metabolite
Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
Application
(s):
insect repellent
An insecticide that acts as a repellent to insects.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
p
-methoxybenzaldehyde (
CHEBI:28235
)
has role
bacterial metabolite (
CHEBI:76969
)
p
-methoxybenzaldehyde (
CHEBI:28235
)
has role
human urinary metabolite (
CHEBI:84087
)
p
-methoxybenzaldehyde (
CHEBI:28235
)
has role
insect repellent (
CHEBI:71692
)
p
-methoxybenzaldehyde (
CHEBI:28235
)
has role
plant metabolite (
CHEBI:76924
)
p
-methoxybenzaldehyde (
CHEBI:28235
)
is a
benzaldehydes (
CHEBI:22698
)
IUPAC Name
4-methoxybenzaldehyde
Synonyms
Sources
4-Anisaldehyde
HMDB
4-Methoxy-Benzaldehyde
HMDB
4-methoxybenzaldehyde
UniProt
Anisal
HMDB
p-Anisaldehyde
KEGG COMPOUND
p-Anisic aldehyde
HMDB
p-Formylanisole
HMDB
p-Methoxybenzaldehyde
HMDB
Para-Anisaldehyde
HMDB
Manual Xrefs
Databases
Anisaldehyde
Wikipedia
C00002636
KNApSAcK
C10761
KEGG COMPOUND
HMDB0029686
HMDB
View more database links
Registry Numbers
Types
Sources
123-11-5
CAS Registry Number
KEGG COMPOUND
123-11-5
CAS Registry Number
NIST Chemistry WebBook
123-11-5
CAS Registry Number
ChemIDplus
471382
Reaxys Registry Number
Reaxys
Citations
Types
Sources
20809147
PubMed citation
Europe PMC
22502535
PubMed citation
Europe PMC
22610435
PubMed citation
Europe PMC
24817361
PubMed citation
Europe PMC
27081359
PubMed citation
Europe PMC
27333544
PubMed citation
Europe PMC
28190358
PubMed citation
Europe PMC
28534578
PubMed citation
Europe PMC
28846628
PubMed citation
Europe PMC
28892803
PubMed citation
Europe PMC
29029251
PubMed citation
Europe PMC
29029346
PubMed citation
Europe PMC
Last Modified
24 September 2021