(-)-Alloaromadendrene

• Catalog No.: 05680
• CAS Number: 25246-27-9
• M. F.: C15H24
• M. W.: 204.35106
• Purity: ≥98.0% (sum of enantiomers, GC)

SYNONYMS

• IUPAC name: (1aS,1bR,2R,4aS,7aR)-1,1,2-trimethyl-5-methylidene-decahydro-1H-cyclopropa[e]azulene
• IUPAC Traditional name: (1aS,1bR,2R,4aS,7aR)-1,1,2-trimethyl-5-methylidene-octahydro-1aH-cyclopropa[e]azulene
• Synonyms: (-)-allo-Aromadendrene

DATABASE IDS

• CAS Number: 25246-27-9
• MDL Number: MFCD16652612
• Beilstein Number: 2357213
• PubChem SID: 24845865

PROPERTIES

• Empirical Formula (Hill Notation): C15H24
• Purity: ≥98.0% (sum of enantiomers, GC)
• Boiling Point: 265-267 °C(lit.)
• Density: 0.923 g/mL at 20 °C(lit.)
• Flash Point: 120 °C
• Flash Point: 248 °F
• Optical Rotation: [α]20/D -33±1°, neat
• Refractive Index: n20/D 1.501
• Personal Protective Equipment: Eyeshields, Gloves
• Storage Temperature: 2-8°C
• German water hazard class: 3

DETAILS

Description (English)

Application
Alloaromadendrene can be used to study chiral building blocks, complex molecules, chemical syntheses and asymmetric syntheses. Alloaromadendrene has been used to apply headspace solid-phase microextraction (HS-SPME) coupled with GC/FID and GC/MS to the analysis of the volatile fraction of an Ephedra species. Alloaromadendrene has also been used to examine the temporal changes of methyl eugenol metabolites in Bactrocera correcta (guava fruit fly) male rectal glands.

Description (简体中文)

Application
Alloaromadendrene can be used to study chiral building blocks, complex molecules, chemical syntheses and asymmetric syntheses. Alloaromadendrene has been used to apply headspace solid-phase microextraction (HS-SPME) coupled with GC/FID and GC/MS to the analysis of the volatile fraction of an Ephedra species. Alloaromadendrene has also been used to examine the temporal changes of methyl eugenol metabolites in Bactrocera correcta (guava fruit fly) male rectal glands.