CHEBI:149671 - (R)-phenylacetylcarbinol

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ChEBI Name (R)-phenylacetylcarbinol ChEBI ID CHEBI:149671 ChEBI ASCII Name (R)-phenylacetylcarbinol Definition A 1-hydroxy-1-phenylpropan-2-one that has (R)-configuration. It is used as a precursor for the production of ephedrine and pseudoephedrine. Stars This entity has been manually annotated by the ChEBI Team. Submitter Anne Morgat 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 C9H10O2 Net Charge 0 Average Mass 150.177 Monoisotopic Mass 150.06808 InChI InChI=1S/C9H10O2/c1-7(10)9(11)8-5-3-2-4-6-8/h2-6,9,11H,1H3/t9-/m0/s1 InChIKey ZBFFNPODXBJBPW-VIFPVBQESA-N SMILES C=1C=CC=CC1[C@H](C(C)=O)O Metabolite of Species Details Saccharomyces cerevisiae (NCBI:txid4932) Found in cell suspension culture (BTO:0000221). See: PubMed Roles Classification Biological Role(s): Saccharomyces cerevisiae metabolite Any fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae ). View more via ChEBI Ontology ChEBI Ontology Outgoing (R)-phenylacetylcarbinol (CHEBI:149671) has role Saccharomyces cerevisiae metabolite (CHEBI:75772) (R)-phenylacetylcarbinol (CHEBI:149671) is a 1-hydroxy-1-phenylpropan-2-one (CHEBI:149767) (R)-phenylacetylcarbinol (CHEBI:149671) is enantiomer of (S)-phenylacetylcarbinol (CHEBI:149670) Incoming rac-phenylacetylcarbinol (CHEBI:149766) has part (R)-phenylacetylcarbinol (CHEBI:149671) (S)-phenylacetylcarbinol (CHEBI:149670) is enantiomer of (R)-phenylacetylcarbinol (CHEBI:149671) IUPAC Name (1R)-1-hydroxy-1-phenylpropan-2-one Synonyms Sources (−)-phenylacetylcarbinol ChemIDplus (1R)-phenylacetylcarbinol ChEBI (R)-(−)-phenylacetylcarbinol ChEBI (R)-1-hydroxy-1-phenyl-2-propanone ChEBI (R)-1-hydroxy-1-phenylacetone ChemIDplus (R)-1-hydroxy-1-phenylpropan-2-one SUBMITTER (R)-PAC MetaCyc (R)-phenylacetylcarbinol UniProt L-PAC ChEBI L-phenylacetylcarbinol ChEBI Manual Xref Database CPD-22734 MetaCyc View more database links Registry Number Type Source 1798-60-3 CAS Registry Number ChemIDplus Citations Types Sources 11759677 PubMed citation Europe PMC 12382047 PubMed citation Europe PMC 12458421 PubMed citation Europe PMC 12889023 PubMed citation Europe PMC 12889791 PubMed citation Europe PMC 12889792 PubMed citation Europe PMC 15219404 PubMed citation Europe PMC 15892055 PubMed citation Europe PMC 16158280 PubMed citation Europe PMC 16685710 PubMed citation Europe PMC 17311582 PubMed citation Europe PMC 24671162 PubMed citation Europe PMC 25424285 PubMed citation Europe PMC 29627855 PubMed citation Europe PMC 31733223 PubMed citation Europe PMC 31950407 PubMed citation Europe PMC IND23338444 Agricola citation Europe PMC IND23338445 Agricola citation Europe PMC IND43992180 Agricola citation Europe PMC IND606859863 Agricola citation Europe PMC Last Modified 18 May 2020