56655

(R)-(−)-3-Hydroxy-valeriansäuremethylester

≥98.0% (sum of enantiomers, GC)

• Synonym(e): (−)-Methyl-(R)-3-hydroxy-valerat
• Empirische Formel (Hill-System): C₆H₁₂O₃
• CAS-Nummer: 60793-22-8
• Molekulargewicht: 132.16
• Beilstein: 4655380
• MDL-Nummer: MFCD00077796
• UNSPSC-Code: 12352108
• PubChem Substanz-ID: 57651591
• NACRES: NA.22

Eigenschaften

• Assay: ≥98.0% (sum of enantiomers, GC)
• Optische Aktivität: [α]20/D −37±3°, c = 1% in chloroform
• Brechungsindex: n20/D 1.427
• bp: 68-70 °C/5 mmHg (lit.)
• Dichte: 1.029 g/mL at 20 °C (lit.)
• SMILES String: CC[C@@H](O)CC(=O)OC
• InChI: 1S/C6H12O3/c1-3-5(7)4-6(8)9-2/h5,7H,3-4H2,1-2H3/t5-/m1/s1
• InChIKey: XHFXKKFVUDJSPJ-RXMQYKEDSA-N

Beschreibung

Anwendung

• Preparation of single-enantiomer 2-methyl-4-heptanol, a pheromone of Metamasius hemipterus, using (S)-2-methoxy-2-(1-naphthyl)propionic acid.: This research outlines the synthesis of a single-enantiomer pheromone compound using (S)-2-methoxy-2-(1-naphthyl)propionic acid. The process highlights the importance of enantiopure intermediates like (−)-Methyl (R)-3-hydroxyvalerate in the synthesis of biologically active compounds (Ichikawa and Ono, 2006).

Sonstige Hinweise

Chiral building block for EPC syntheses; selective anti-alkylation of its dianion; OH protection and reduction of ester group to aldehyde or alcohol functions; stereoselective preparation of a dioxanone with pivalaldehyde

Sicherheitshinweise

• Lagerklassenschlüssel: 10 - Combustible liquids
• WGK: WGK 3
• Flammpunkt (°F): 168.8 °F - closed cup
• Flammpunkt (°C): 76 °C - closed cup
• Persönliche Schutzausrüstung: Eyeshields, Gloves, type ABEK (EN14387) respirator filter