CHEBI:62952 - aminocyclopyrachlor

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ChEBI Name aminocyclopyrachlor
ChEBI ID CHEBI:62952
Definition An organochlorine herbicide, the structure of which is that of pyrimidine-4-carboxylic acid substituted at positions 2, 5 and 6 by cyclopropyl, chloro and amino groups respectively.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C8H8ClN3O2
Net Charge 0
Average Mass 213.62100
Monoisotopic Mass 213.03050
InChI InChI=1S/C8H8ClN3O2/c9-4-5(8(13)14)11-7(3-1-2-3)12-6(4)10/h3H,1-2H2,(H,13,14)(H2,10,11,12)
InChIKey KWAIHLIXESXTJL-UHFFFAOYSA-N
SMILES Nc1nc(nc(C(O)=O)c1Cl)C1CC1
Roles Classification
Biological Role(s): synthetic auxin
A synthetic compound exhibiting auxin activity.
Application(s): herbicide
A substance used to destroy plant pests.
pesticide
Strictly, a substance intended to kill pests. In common usage, any substance used for controlling, preventing, or destroying animal, microbiological or plant pests.
(via organochlorine pesticide )
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ChEBI Ontology
Outgoing aminocyclopyrachlor (CHEBI:62952) has part primary amino group (CHEBI:46882)
aminocyclopyrachlor (CHEBI:62952) has role herbicide (CHEBI:24527)
aminocyclopyrachlor (CHEBI:62952) has role synthetic auxin (CHEBI:26841)
aminocyclopyrachlor (CHEBI:62952) is a cyclopropanes (CHEBI:51454)
aminocyclopyrachlor (CHEBI:62952) is a organochlorine pesticide (CHEBI:38656)
aminocyclopyrachlor (CHEBI:62952) is a pyrimidines (CHEBI:39447)
aminocyclopyrachlor (CHEBI:62952) is conjugate acid of aminocyclopyrachlor(1−) (CHEBI:62954)
Incoming aminocyclopyrachlor-methyl (CHEBI:63215) has functional parent aminocyclopyrachlor (CHEBI:62952)
aminocyclopyrachlor(1−) (CHEBI:62954) is conjugate base of aminocyclopyrachlor (CHEBI:62952)
IUPAC Name
6-amino-5-chloro-2-cyclopropylpyrimidine-4-carboxylic acid
Synonyms Sources
6-amino-5-chloro-2-cyclopropyl-4-pyrimidinecarboxylic acid ChEBI
aminocyclopyrachlore ChEBI
Brand Name Source
Imprelis ChEBI
Manual Xrefs Databases
1668 PPDB
Aminocyclopyrachlor Wikipedia
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Registry Numbers Types Sources
11329725 Reaxys Registry Number Reaxys
858956-08-8 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
19063674 PubMed citation Europe PMC
21384924 PubMed citation Europe PMC
21594961 PubMed citation Europe PMC
IND44360965 Agricola citation Europe PMC
IND44360966 Agricola citation Europe PMC
Last Modified
10 September 2013