
Aclonifen
Aclonifen is a primary amino compound that is aniline in which the phenyl group has been substituted at positions 2, 3, and 6 by chlorine, phenoxy, and nitro groups, respectively. A protoporphyrinogen oxidase (PPO) inhibitor, it is used as a herbicide against a broad range of weeds in a wide range of crops. It has a role as a carotenoid biosynthesis inhibitor, a herbicide, an agrochemical and an EC 1.3.3.4 (protoporphyrinogen oxidase) inhibitor. It is an aromatic ether, a C-nitro compound, a substituted aniline, a primary amino compound and a member of monochlorobenzenes. — ChEBI
- IUPAC name
- 2-chloro-6-nitro-3-phenoxyaniline
- Molecular formula
- C12H9ClN2O3
- Molecular weight
- 264.66 g/mol
- Exact mass
- 264.0301698 Da
- XLogP3
- 3.8
- Topological polar surface area
- 81.1 Ų
- Hydrogen-bond donors
- 1
- Hydrogen-bond acceptors
- 4
- Covalent units
- 1
- Defined stereocentres
- 0
Also known as
16 more reported names
External database identifiers
- ChEBI:CHEBI:137374
- ChEMBL:CHEMBL1485557
- EPA DTXSID:DTXSID7058175
- PubMed:28927721
- PubMed:20369492
- PubMed:19382587
- PubMed:17390816
- PubMed:17390814
- PubMed:17313105
- PubMed:12558095
Retrieved from NIH PubChem on 2026-09-02 by checksum-valid CAS matching. Chemical properties do not replace the regulatory decision on this page.