Structure via PubChem · Public domain (PubChem)
(+/-)-phenylacetylcarbinol
Sign in to savethumb|L-pac produced by biotransformation of benzaldehyde Phenylacetylcarbinol (PAC) is an organic compound that has two enantiomers, one with R- and one with S-configuration. (R)-PAC, which is commonly called -PAC, is known as a precursor in the synthesis of pharmaceuticals such as ephedrine and pseudoephedrine.
Chemical data
- Formula
- C9H10O2
- Molecular weight
- 150.17 g/mol
- IUPAC name
- 1-hydroxy-1-phenylpropan-2-one
- SMILES
- CC(=O)C(C1=CC=CC=C1)O
- InChIKey
- ZBFFNPODXBJBPW-UHFFFAOYSA-N
- XLogP
- 1
- Polar surface area
- 37.3 Ų
- H-bond donors
- 1
- H-bond acceptors
- 2
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Molecule type
- Small molecule
via ChEMBL · EBI
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 150.068
Show 3 more facts
- chemical formula
- C₉H₁₀O₂
- canonical SMILES
- CC(=O)C(C1=CC=CC=C1)O
- Commons category
- Phenylacetylcarbinol
Sources (2)
via Wikidata · CC0
~2 min read
Encyclopedic overview
3 sectionsContents
- Nomenclature
- Production
- References
thumb|L-pac produced by biotransformation of benzaldehyde Phenylacetylcarbinol (PAC) is an organic compound that has two enantiomers, one with R- and one with S-configuration. (R)-PAC, which is commonly called -PAC, is known as a precursor in the synthesis of pharmaceuticals such as ephedrine and pseudoephedrine.
== Nomenclature ==
Excerpted from Wikipedia’s “(+/-)-phenylacetylcarbinol” article, available under the CC BY-SA 4.0 licence.