Geranyl Linalool

CAS : 1113-21-9

Ref. TR-G367750

Informations sur le produit

• Nom: Geranyl Linalool
• Synonymes: 3,7,11,15-Tetramethyl-1,6,10,14-hexadecatetraen-3-ol, 3,7,11,15-Tetramethyl-1,6,10,14-cetene-3-ol, 3,7,11,15-Tetramethyl-3-hydroxy-1,6,10,14-hexadecatetraene, (6E)-3,7,11,15-Tetramethylhexadeca-1,6,10,14-tetraen-3-ol, (6E,10E)-3,7,11,15-Tetramethyl-1,6,10,14-hexadecatetraen-3-ol, (6E,10E)-3,7,11,15-Tetramethylhexadeca-1,6,10,14-tetraen-3-ol, (E,E)-3,7,11,15-Tetramethyl-1,6,10,14-Hexadecatetraen-3-ol, (E,E)-Geranyllinalool, (±)-Geranyllinalool, 1,6,10,14-Hexadecatetraen-3-ol, 3,7,11,15-tetramethyl-, (E,E)-, 1,6,10,14-hexadecatetraen-3-ol, 3,7,11,15-tetramethyl-, (6E)-, 1,6,10,14-hexadecatetraen-3-ol, 3,7,11,15-tetramethyl-, (6E,10E)-, Geranyl inalool, Geranyl linalool, Linalool, geranyl-
• CAS: 1113-21-9

Description

Applications Geranyl Linalool is am aliphatic genaryl derivative. Geranyl Linalool unlike other genaryl derivatives showed poor inhibitory activity against carotenoid synthesis in Synechococcus. Geranyl Linalool was identified as a testosterone-dependent volatile compound in the preputial gland of rat Rattus norvegicus.
References Juettner, F. et al.: Zeitsch. Naturforsch. C J. Biosci., 38C, 387 (1983); Ponmanickam, P. et al.: Gen. Comp. Endocrinol., 167, 35 (2010):

• Marque: TRC

Propriétés chimiques

• Masse moléculaire: 290.48
• Formule: C₂₀H₃₄O
• Couleur/Forme: Neat
• InChI: InChI=1S/C20H34O/c1-7-20(6,21)16-10-15-19(5)14-9-13-18(4)12-8-11-17(2)3/h7,11,13,15,21H,1,8-10,12,14,16H2,2-6H3/b18-13+,19-15+
• Code InChI: InChIKey=IQDXAJNQKSIPGB-HQSZAHFGSA-N
• SMILES: C=CC(C)(O)CC/C=C(\C)CC/C=C(\C)CCC=C(C)C