CHEBI:75703 - (R)-mecoprop

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ChEBI Name (R)-mecoprop
ChEBI ID CHEBI:75703
ChEBI ASCII Name (R)-mecoprop
Definition The (R)-enantiomer of 2-(4-chloro-2-methylphenoxy)propanoic acid; the active stereoisomer of the racemic herbicide mecoprop.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information ChemicalBook:CB8188959, eMolecules:501705, ZINC000000256144
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Formula C10H11ClO3
Net Charge 0
Average Mass 214.64600
Monoisotopic Mass 214.03967
InChI InChI=1S/C10H11ClO3/c1-6-5-8(11)3-4-9(6)14-7(2)10(12)13/h3-5,7H,1-2H3,(H,12,13)/t7-/m1/s1
InChIKey WNTGYJSOUMFZEP-SSDOTTSWSA-N
SMILES C[C@@H](Oc1ccc(Cl)cc1C)C(O)=O
Roles Classification
Chemical Role(s): Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
Application(s): phenoxy herbicide
Any member of the class of herbicides whose members contain a phenoxy or substituted phenoxy group.
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ChEBI Ontology
Outgoing (R)-mecoprop (CHEBI:75703) has role phenoxy herbicide (CHEBI:60575)
(R)-mecoprop (CHEBI:75703) is a 2-(4-chloro-2-methylphenoxy)propanoic acid (CHEBI:75704)
(R)-mecoprop (CHEBI:75703) is conjugate acid of (R)-2-(4-chloro-2-methylphenoxy)propanoate (CHEBI:75284)
(R)-mecoprop (CHEBI:75703) is enantiomer of (S)-mecoprop (CHEBI:75712)
Incoming mecoprop (CHEBI:75711) has part (R)-mecoprop (CHEBI:75703)
(R)-2-(4-chloro-2-methylphenoxy)propanoate (CHEBI:75284) is conjugate base of (R)-mecoprop (CHEBI:75703)
(S)-mecoprop (CHEBI:75712) is enantiomer of (R)-mecoprop (CHEBI:75703)
IUPAC Name
(2R)-2-(4-chloro-2-methylphenoxy)propanoic acid
Synonyms Sources
(+)-Mcpp ChemIDplus
(2R)-2-(4-chloro-2-methylphenoxy)propionic acid ChEBI
(R)-2-(4-chloro-2-methylphenoxy)propanoic acid ChEBI
(R)-2-(4-chloro-o-tolyloxy)propionic acid KEGG COMPOUND
(R)-MCPP ChEBI
2M-4XP ChemIDplus
d-Mecoprop ChemIDplus
Mecoprop-P KEGG COMPOUND
Manual Xrefs Databases
431 PPDB
C18608 KEGG COMPOUND
CA2703613 Patent
Mecoprop Wikipedia
mecoprop-p Alan Wood's Pesticides
WO2009053063 Patent
WO2010017929 Patent
View more database links
Registry Numbers Types Sources
16484-77-8 CAS Registry Number ChemIDplus
1960621 Reaxys Registry Number Reaxys
Citations Waiting for Citations
Last Modified
18 November 2019