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> Main
CHEBI:3751 - clomazone
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ChEBI Name
clomazone
ChEBI ID
CHEBI:3751
Definition
An isoxazolidinone that is 1,2-oxazolidin-3-one substituted by a 2-chlorobenzyl group at position 2 and two methyl groups at position 4.
Stars
This entity has been manually annotated by the ChEBI Team.
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Formula
C12H14ClNO2
Net Charge
0
Average Mass
239.698
Monoisotopic Mass
239.07131
InChI
InChI=1S/C12H14ClNO2/c1-12(2)8-16-14(11(12)15)7-9-5-3-4-6-10(9)13/h3-6H,7-8H2,1-2H3
InChIKey
KIEDNEWSYUYDSN-UHFFFAOYSA-N
SMILES
C1ON(CC=2C=CC=CC2Cl)C(C1(C)C)=O
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.
carotenoid biosynthesis inhibitor
Any pathway inhibitor that acts on the carotenoid biosynthesis pathway.
Application
(s):
herbicide
A substance used to destroy plant pests.
agrochemical
An agrochemical is a substance that is used in agriculture or horticulture.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
clomazone (
CHEBI:3751
)
has role
agrochemical (
CHEBI:33286
)
clomazone (
CHEBI:3751
)
has role
carotenoid biosynthesis inhibitor (
CHEBI:138208
)
clomazone (
CHEBI:3751
)
has role
environmental contaminant (
CHEBI:78298
)
clomazone (
CHEBI:3751
)
has role
herbicide (
CHEBI:24527
)
clomazone (
CHEBI:3751
)
has role
xenobiotic (
CHEBI:35703
)
clomazone (
CHEBI:3751
)
is a
isoxazolidinone (
CHEBI:55375
)
clomazone (
CHEBI:3751
)
is a
monochlorobenzenes (
CHEBI:83403
)
IUPAC Name
2-(2-chlorobenzyl)-4,4-dimethyl-1,2-oxazolidin-3-one
Synonyms
Sources
Dimethazone
NIST Chemistry WebBook
FMC57020
KEGG COMPOUND
Manual Xrefs
Databases
168
PPDB
C11095
KEGG COMPOUND
clomazone
Alan Wood's Pesticides
Clomazone
Wikipedia
View more database links
Registry Numbers
Types
Sources
7480026
Reaxys Registry Number
Reaxys
81777-89-1
CAS Registry Number
NIST Chemistry WebBook
Citations
Types
Sources
21191867
PubMed citation
Europe PMC
23538322
PubMed citation
Europe PMC
24515809
PubMed citation
Europe PMC
24562457
PubMed citation
Europe PMC
24792474
PubMed citation
Europe PMC
25380132
PubMed citation
Europe PMC
25779373
PubMed citation
Europe PMC
26370279
PubMed citation
Europe PMC
27332840
PubMed citation
Europe PMC
28458150
PubMed citation
Europe PMC
28719874
PubMed citation
Europe PMC
32625947
PubMed citation
Europe PMC
33640824
PubMed citation
Europe PMC
34446194
PubMed citation
Europe PMC
36688907
PubMed citation
Europe PMC
36778854
PubMed citation
Europe PMC
Last Modified
22 March 2023