Services
Research
Training
Industry
About us
ChEBI
Examples:
iron*
,
InChI=1S/CH4O/c1-2/h2H,1H3
,
caffeine
Advanced
Home
Advanced Search
Browse
Documentation
Download
Tools
About ChEBI
Submit
Contact us
DiNA
Statistics
Entity of the Month
Periodic Table
Ontology
Train online
User Manual
Annotation Manual
Developer Manual
FAQ's
BiNChE
libChEBI
Web Services
ChEBI
> Main
CHEBI:16562 - 2-phenylacetamide
Main
ChEBI Ontology
Automatic Xrefs
Reactions
Pathways
Models
ChEBI Name
2-phenylacetamide
ChEBI ID
CHEBI:16562
Definition
A monocarboxylic acid amide that is acetamide substituted by a phenyl group at position 2.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:11647, CHEBI:19762, CHEBI:1264, CHEBI:25974
Supplier Information
Download
Molfile
XML
SDF
Find compounds which contain this structure
Find compounds which resemble this structure
Take structure to the Advanced Search
more structures >>
Molfile
Formula
C8H9NO
Net Charge
0
Average Mass
135.16320
Monoisotopic Mass
135.06841
InChI
InChI=1S/C8H9NO/c9-8(10)6-7-4-2-1-3-5-7/h1-5H,6H2,(H2,9,10)
InChIKey
LSBDFXRDZJMBSC-UHFFFAOYSA-N
SMILES
NC(=O)Cc1ccccc1
Metabolite of Species
Details
Mus musculus
(NCBI:txid10090)
Source: BioModels - MODEL1507180067 See:
PubMed
Roles Classification
Biological Role
(s):
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (
Mus musculus
).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
2-phenylacetamide (
CHEBI:16562
)
has functional parent
phenylacetic acid (
CHEBI:30745
)
2-phenylacetamide (
CHEBI:16562
)
has role
mouse metabolite (
CHEBI:75771
)
2-phenylacetamide (
CHEBI:16562
)
is a
monocarboxylic acid amide (
CHEBI:29347
)
IUPAC Name
2-phenylacetamide
Synonyms
Sources
2-Phenylacetamide
KEGG COMPOUND
2-phenylacetamide
UniProt
α-phenylacetamide
NIST Chemistry WebBook
α-toluamide
NIST Chemistry WebBook
benzeneacetamide
NIST Chemistry WebBook
phenyl-β-acetylamine
NIST Chemistry WebBook
phenylacetamide
UM-BBD
phenylacetic acid amide
ChemIDplus
Manual Xrefs
Databases
C02505
KEGG COMPOUND
c0648
UM-BBD
CPD-238
MetaCyc
HMDB0010715
HMDB
View more database links
Registry Numbers
Types
Sources
101820
Gmelin Registry Number
Gmelin
103-81-1
CAS Registry Number
KEGG COMPOUND
103-81-1
CAS Registry Number
ChemIDplus
103-81-1
CAS Registry Number
NIST Chemistry WebBook
507886
Beilstein Registry Number
Beilstein
507886
Reaxys Registry Number
Reaxys
Citation
Type
Source
22548364
PubMed citation
Europe PMC
Last Modified
21 July 2020