62139

(−)-Linalool

≥95.0% (sum of enantiomers, GC)

• Synonym(e): (R)-(−)-3,7-Dimethyl-1,6-octadien-3-ol
• Lineare Formel: (CH₃)₂C=CHCH₂CH₂C(CH₃)(OH)CH=CH₂
• CAS-Nummer: 126-91-0
• Molekulargewicht: 154.25
• Beilstein: 1721487
• EG-Nummer: 204-811-2
• MDL-Nummer: MFCD00135469
• UNSPSC-Code: 12352002
• PubChem Substanz-ID: 57651876
• NACRES: NA.22

Eigenschaften

• Qualitätsniveau: 100
• Assay: ≥95.0% (sum of enantiomers, GC)
• Optische Aktivität: [α]20/D −18±3°, neat
• Brechungsindex: n20/D 1.4615 (lit.); n20/D 1.462
• bp: 198 °C (lit.)
• Dichte: 0.862 g/mL at 20 °C (lit.)
• Funktionelle Gruppe: hydroxyl
• SMILES String: C\C(C)=C\CC[C@@](C)(O)C=C
• InChI: 1S/C10H18O/c1-5-10(4,11)8-6-7-9(2)3/h5,7,11H,1,6,8H2,2-4H3/t10-/m0/s1
• InChIKey: CDOSHBSSFJOMGT-JTQLQIEISA-N

Beschreibung

Allgemeine Beschreibung

(-)-Linalool is a monoterpene compound mainly found in many essential oils. It shows anti-nociceptive and anti-inflammatory activity.

Anwendung

(-)-Linalool can be used as a reactant in:

• The enantioselective preparation of ophiobolin sesterterpene via diastereoselective reductive radical cascade cyclization.
• The total synthesis of (-)-5,6-dihydrocineromycin B via (-)-linalool O-triethylsilyl ether.;
• The total synthesis of pladienolide B analog.

Sicherheitshinweise

• Piktogramme: GHS07
• Signalwort: Warning
• H-Sätze: H315,H317,H319,H335
• P-Sätze: P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338
• Gefahreneinstufungen: Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3
• Zielorgane: Respiratory system
• Lagerklassenschlüssel: 10 - Combustible liquids
• WGK: WGK 3
• Flammpunkt (°F): 166.3 °F - closed cup
• Flammpunkt (°C): 74.6 °C - closed cup
• Persönliche Schutzausrüstung: Eyeshields, Gloves, type ABEK (EN14387) respirator filter