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:18112 - 2-aminophenol
Main
ChEBI Ontology
Automatic Xrefs
Reactions
Pathways
Models
ChEBI Name
2-aminophenol
ChEBI ID
CHEBI:18112
Definition
The aminophenol which has the single amino substituent located
ortho
to the phenolic -OH group.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:39779, CHEBI:11527, CHEBI:1023, CHEBI:19476
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
expand
Wikipedia
License
Read full article at Wikipedia
Formula
C6H7NO
Net Charge
0
Average Mass
109.12592
Monoisotopic Mass
109.05276
InChI
InChI=1S/C6H7NO/c7-5-3-1-2-4-6(5)8/h1-4,8H,7H2
InChIKey
CDAWCLOXVUBKRW-UHFFFAOYSA-N
SMILES
Nc1ccccc1O
Roles Classification
Chemical Role
(s):
Bronsted base
A molecular entity capable of accepting a hydron from a donor (Br
o
nsted acid).
(via
organic amino compound
)
Biological Role
(s):
bacterial metabolite
Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
2-aminophenol (
CHEBI:18112
)
has role
bacterial metabolite (
CHEBI:76969
)
2-aminophenol (
CHEBI:18112
)
is a
aminophenol (
CHEBI:28829
)
Incoming
2-acetamidophenol sulfate (
CHEBI:133562
)
has functional parent
2-aminophenol (
CHEBI:18112
)
2-aminophenyl hydrogen sulfate (
CHEBI:133186
)
has functional parent
2-aminophenol (
CHEBI:18112
)
IUPAC Name
2-aminophenol
Synonyms
Sources
2-Aminobenzenol
KEGG COMPOUND
2-Aminophenol
KEGG COMPOUND
2-AMINOPHENOL
PDBeChem
2-aminophenol
UniProt
2-Hydroxyaniline
KEGG COMPOUND
o-Aminophenol
KEGG COMPOUND
o
-hydroxyaniline
NIST Chemistry WebBook
Manual Xrefs
Databases
2-Aminophenol
Wikipedia
2AF
PDBeChem
C00007533
KNApSAcK
C01987
KEGG COMPOUND
c0316
UM-BBD
DB01726
DrugBank
View more database links
Registry Numbers
Types
Sources
26978
Gmelin Registry Number
Gmelin
606075
Gmelin Registry Number
Gmelin
606075
Reaxys Registry Number
Reaxys
95-55-6
CAS Registry Number
KEGG COMPOUND
95-55-6
CAS Registry Number
ChemIDplus
95-55-6
CAS Registry Number
NIST Chemistry WebBook
Citations
Types
Sources
11304127
PubMed citation
Europe PMC
1395635
PubMed citation
Europe PMC
24124510
PubMed citation
Europe PMC
24571346
PubMed citation
Europe PMC
9683650
PubMed citation
Europe PMC
Last Modified
03 October 2016