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:67128 - 2,4-dinitro-1-naphthol
Main
ChEBI Ontology
Automatic Xrefs
Reactions
Pathways
Models
ChEBI Name
2,4-dinitro-1-naphthol
ChEBI ID
CHEBI:67128
Definition
A naphthol in which the hydroxy substituent is at C-1 with nitro groups at C-2 and -4.
Stars
This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download
Molfile
XML
SDF
Find compounds which contain this structure
Find compounds which resemble this structure
Take structure to the Advanced Search
Wikipedia
License
Read full article at Wikipedia
Formula
C10H6N2O5
Net Charge
0
Average Mass
234.16500
Monoisotopic Mass
234.02767
InChI
InChI=1S/C10H6N2O5/c13-10-7-4-2-1-3-6(7)8(11(14)15)5-9(10)12(16)17/h1-5,13H
InChIKey
FFRBMBIXVSCUFS-UHFFFAOYSA-N
SMILES
Oc1c(cc([N+]([O-])=O)c2ccccc12)[N+]([O-])=O
Roles Classification
Application
(s):
histological dye
A dye used in microscopic or electron microscopic examination of cells and tissues to give contrast and to highlight particular features of interest, such as nuclei and cytoplasm.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
2,4-dinitro-1-naphthol (
CHEBI:67128
)
has role
histological dye (
CHEBI:77178
)
2,4-dinitro-1-naphthol (
CHEBI:67128
)
is a
C
-nitro compound (
CHEBI:35716
)
2,4-dinitro-1-naphthol (
CHEBI:67128
)
is a
naphthols (
CHEBI:25392
)
IUPAC Name
2,4-dinitronaphthalen-1-ol
Synonyms
Sources
2,4-dinitro-1-hydroxynaphthalene
ChEBI
2,4-dinitro-α-naphthol
ChEBI
2,4-dinitronaphthalenol
ChEBI
acid yellow 24
ChEBI
C.I. 10315
ChEBI
Golden yellow
ChemIDplus
Manchester Yellow
ChemIDplus
Martius yellow
ChemIDplus
Naphthol yellow
ChEBI
Naphthylene Yellow
ChemIDplus
Saffron Yellow
ChemIDplus
Manual Xref
Database
Martius_yellow
Wikipedia
View more database links
Registry Numbers
Types
Sources
2057462
Reaxys Registry Number
Reaxys
2057462
Beilstein Registry Number
Beilstein
605-69-6
CAS Registry Number
NIST Chemistry WebBook
605-69-6
CAS Registry Number
ChemIDplus
Citation
Type
Source
1650428
PubMed citation
Europe PMC
Last Modified
04 November 2015