CAS 1798-60-3

(R)-Phenylacetylcarbinol

Formula: C₉H₁₀O₂

InChI: InChI=1S/C9H10O2/c1-7(10)9(11)8-5-3-2-4-6-8/h2-6,9,11H,1H3/t9-/m0/s1

InChI key: InChIKey=ZBFFNPODXBJBPW-VIFPVBQESA-N

SMILES: [C@@H](C(C)=O)(O)C1=CC=CC=C1

Synonyms:

• (-)-(1R)-1-Hydroxy-1-phenyl-2-propanone
• (1R)-1-Phenyl-1-hydroxypropan-2-one
• (1R)-1-hydroxy-1-phenylpropan-2-one
• (R)-1-Hydroxy-1-phenyl-2-propanone
• (R)-1-Hydroxy-1-phenylpropanone
• (R)-Hydroxy-1-Phenyl-2-propanedione
• (R)-Phenylacetylcarbinol
• 1-Hydroxy-1-Phenylpropan-2-One
• 2-Propanone, 1-hydroxy-1-phenyl-, (1R)-
• 2-Propanone, 1-hydroxy-1-phenyl-, (R)-
• <span class="text-smallcaps">D</span>-(-)-1-Hydroxy-1-phenylpropanone
• <span class="text-smallcaps">D</span>-(-)-1-Phenyl-1-hydroxy-2-propanone
• <span class="text-smallcaps">D</span>-(-)-Phenylacetylcarbinol
• l-Phenylacetylcarbinol
• D-(-)-1-Hydroxy-1-phenylpropanone

(R)-1-Hydroxy-1-phenylpropanone

Controlled Product

CAS: 1798-60-3

Applications (R)-1-Hydroxy-1-phenylpropanone is used as a reagent in the preparation of chiral (amino)alkanol derivatives and determination of their activity as antibacterial agents and antifungal agents. It is also an intermediate used in the synthesis of Pseudoephedrine and Ephedrine.
References Chennakesava, R. K., et al.: Bioorg. Med. Chem. Lett., 24, 3057 (2014); Baxter, E., et al.: Org. Reactions, 59 (2002); Astrova, M., et al.: Res. on Chem. Intermediates, 33, 663 (2007)

Formula: C₉H₁₀O₂

Color and Shape: Neat

Molecular weight: 150.17

Ref: TR-H949610

Ephedrine Hydrochloride EP Impurity A

Controlled Product

CAS: 1798-60-3

Ephedrine Hydrochloride EP Impurity A is a product of the biotransformations of pseudoephedrine. It has been shown that this impurity can be formed in enzymatic reactions where pseudoephedrine is acted upon by β-unsaturated ketones or by filamentous fungi. Ephedrine Hydrochloride EP Impurity A is a chiral compound, which means that it has two different forms that are non-superimposable mirror images of each other. The enantiomers (left and right) are the individual molecules that make up the racemic mixture. In some cases, ephedrine hydrochloride ep impurity a may be present as a result of a reaction between pseudoephedrine and an enzyme preparation containing β-unsaturated ketones, such as acetone peroxide or benzoyl peroxide. This impurity has been shown to inhibit candida glabrata and to have kinetic properties similar to that of ephed

Formula: C₉H₁₀O₂

Purity: Min. 96 Area-%

Color and Shape: Clear Viscous Liquid

Molecular weight: 150.17 g/mol

Ref: 3D-IE176322

Ephedrine EP Impurity A

Controlled Product

CAS: 1798-60-3

Formula: C₉H₁₀O₂

Molecular weight: 150.18

Ref: ST-EA-CP-E122001