CHEBI:75712 - (S)-mecoprop

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ChEBI Name (S)-mecoprop ChEBI ID CHEBI:75712 ChEBI ASCII Name (S)-mecoprop Definition The (S)-enantiomer of 2-(4-chloro-2-methylphenoxy)propanoic acid; the inactive stereoisomer of the racemic herbicide mecoprop. Stars This entity has been manually annotated by the ChEBI Team. Supplier Information Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search 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-/m0/s1 InChIKey WNTGYJSOUMFZEP-ZETCQYMHSA-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 ) View more via ChEBI Ontology ChEBI Ontology Outgoing (S)-mecoprop (CHEBI:75712) is a 2-(4-chloro-2-methylphenoxy)propanoic acid (CHEBI:75704) (S)-mecoprop (CHEBI:75712) is conjugate acid of (S)-2-(4-chloro-2-methylphenoxy)propanoate (CHEBI:75285) (S)-mecoprop (CHEBI:75712) is enantiomer of (R)-mecoprop (CHEBI:75703) Incoming mecoprop (CHEBI:75711) has part (S)-mecoprop (CHEBI:75712) (S)-2-(4-chloro-2-methylphenoxy)propanoate (CHEBI:75285) is conjugate base of (S)-mecoprop (CHEBI:75712) (R)-mecoprop (CHEBI:75703) is enantiomer of (S)-mecoprop (CHEBI:75712) Synonym Source (S)-MCPP ChEBI Registry Number Type Source 3201761 Reaxys Registry Number Reaxys Last Modified 24 September 2013