Compound
1-chloro-2,4-dinitrobenzene
A skin irritant that may cause dermatitis of both primary and allergic types. Contact sensitization with dncb has been used as a measure of cellular immunity. Dncb is also used as a reagent for the detection and determination of pyridine compounds.
CHEBI:34718ChEBI
Structure
Loading the model…
- Class
- Organic compound
- Formula
- C6H3ClN2O4
- Mass
- 202.553 g/mol
- Charge
- 0
- InChIKey
- VYZAHLCBVHPDDF-UHFFFAOYSA-N
- SMILES
- O=[N+]([O-])c1ccc(Cl)c([N+](=O)[O-])c1
- Look it up
- ChEBIPubChemBy InChIKey
Identity from ChEBI, geometry from PubChem. Not evidence.
What it touches on the way
Mechanistic reach
3 entities
3 entities reached.
What the reference databases state
Statements
4 statements
4 statements · 1 reference database · Subject: 1-chloro-2,4-dinitrobenzene · Sources: Rhea
- 1-chloro-2,4-dinitrobenzene is metabolised by GSTM4ProteinRhea RHEA:51220Inferred only
- 1-chloro-2,4-dinitrobenzene is a substrate of LANCL1ProteinRhea RHEA:51220Inferred only
- 1-chloro-2,4-dinitrobenzene is a substrate of MGST2ProteinRhea RHEA:51220Inferred only
- 1-chloro-2,4-dinitrobenzene is a substrate of PTGESProteinRhea RHEA:51220Inferred only
Reactions
1 reaction
1-chloro-2,4-dinitrobenzene+glutathione2,4-dinitrophenyl-S-glutathione+chloride+hydron
Catalysed by PTGES or LANCL1 or GSTM4 or MGST2
Reaction pageLeft to rightBalanced
Rhea RHEA:51220CC BY 4.0Reference data
Other names
12 names
Resolves to: 1-chloro-2,4-dinitrobenzene
- Also called
- 1,3-Dinitro-4-chlorobenzene2,4-Dinitro-1-chlorobenzene2,4-Dinitrochlorobenzene2,4-Dinitrophenyl chloride4-Chloro-1,3-dinitrobenzene6-Chloro-1,3-dinitrobenzeneCdnbChlorodinitrobenzeneClDNBDinitrochlorobenzeneDncbDNPCl