CHEBI:19503 - propachlor

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ChEBI Name propachlor
ChEBI ID CHEBI:19503
Definition An anilide that consists of 2-chloroacetanilide bearing an N-isopropyl substituent.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C11H14ClNO
Net Charge 0
Average Mass 211.68800
Monoisotopic Mass 211.07639
InChI InChI=1S/C11H14ClNO/c1-9(2)13(11(14)8-12)10-6-4-3-5-7-10/h3-7,9H,8H2,1-2H3
InChIKey MFOUDYKPLGXPGO-UHFFFAOYSA-N
SMILES CC(C)N(C(=O)CCl)c1ccccc1
Roles Classification
Chemical Role(s): environmental contaminant
Any minor or unwanted substance introduced into the environment that can have undesired effects.
Biological Role(s): xenobiotic
A xenobiotic (Greek, xenos "foreign"; bios "life") is a compound that is foreign to a living organism. Principal xenobiotics include: drugs, carcinogens and various compounds that have been introduced into the environment by artificial means.
Application(s): herbicide
A substance used to destroy plant pests.
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ChEBI Ontology
Outgoing propachlor (CHEBI:19503) has role environmental contaminant (CHEBI:78298)
propachlor (CHEBI:19503) has role herbicide (CHEBI:24527)
propachlor (CHEBI:19503) has role xenobiotic (CHEBI:35703)
propachlor (CHEBI:19503) is a anilide (CHEBI:13248)
propachlor (CHEBI:19503) is a monocarboxylic acid amide (CHEBI:29347)
propachlor (CHEBI:19503) is a organochlorine compound (CHEBI:36683)
IUPAC Name
2-chloro-N-isopropyl-N-phenylacetamide
Synonyms Sources
2-Chloro-N-(1-methylethyl)-N-phenylacetamide ChemIDplus
2-chloro-N-isopropylacetanilide ChEBI
α-chloro-N-isopropylacetanilid NIST Chemistry WebBook
alpha-Chloro-N-isopropylacetanilide ChemIDplus
Chloressigsäure-N-isopropylanilid ChemIDplus
N-isopropyl-2-chloroacetanilide ChEBI
N-isopropyl-α-chloroacetanilide UM-BBD
Brand Names Sources
Bexton 4L ChemIDplus
Kartex A ChemIDplus
Nitacid ChemIDplus
Niticid ChemIDplus
Propachlore ChemIDplus
Ramrod 65 ChemIDplus
Manual Xrefs Databases
543 PPDB
c0653 UM-BBD
C18759 KEGG COMPOUND
propachlor Alan Wood's Pesticides
Propachlor Wikipedia
View more database links
Registry Numbers Types Sources
1918-16-7 CAS Registry Number KEGG COMPOUND
1918-16-7 CAS Registry Number NIST Chemistry WebBook
1918-16-7 CAS Registry Number ChemIDplus
2103903 Beilstein Registry Number ChemIDplus
2103903 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
22953837 PubMed citation Europe PMC
7272464 PubMed citation Europe PMC
Last Modified
10 November 2014
General Comment
2014-10-29 Stravs M, Schymanski E, Singer H, Department of Environmental Chemistry, Eawag