(2E,6E)-3,7,11-Trimethyldodeca-2,6,10-trien-1-yl Acetate

CAS : 4128-17-0

Ref. TR-T796695

Informations sur le produit

• Nom: (2E,6E)-3,7,11-Trimethyldodeca-2,6,10-trien-1-yl Acetate
• Synonymes: (2E,6E)-3,7,11-Trimethyl-2,6,10-dodecatrien-1-ol 1-Acetate, (2E,6E)-3,7,11-Trimethyl-2,6,10-dodecatrien-1-ol Acetate, (E,E)-3,7,11-Trimethyl-2,6,10-dodecatrien-1-ol Acetate, (2E,6E)-Farnesyl Acetate,(E,E)-Farnesyl Acetate, 2-trans-6-trans-Farnesyl Acetate, Acetic Acid (2E,6E)-3,7,11-Trimethyl-2,6,10-dodecatrienyl Ester, Acetic Acid Farnesyl Ester,all-trans-Farnesyl Acetate, trans,trans-Farnesol Acetate, trans,trans-Farnesyl Acetate,trans-2-trans-6-Farnesyl Acetate
• Marque: TRC
• Description: Applications (2E,6E)-3,7,11-Trimethyldodeca-2,6,10-trien-1-yl Acetate is an intermediate in the synthesis of JHSB3 (J211030). JHSB3 is an acyclic sesquiterpenoid that regulates many aspects of insect physiology. Juvenile Hormone regulate development, reproduction, diapause, and polyphenisms.References Kotaki, T., et al.: Org. Let., 11, 5234 (2009); Riddiford, L.: Adv. Insect Physiol., 24, 213 (1994); Wyatt, G., Davey, K.: Adv. Insect Physiol., 26, 1 (1996); Nijhout, H.: Insect Hormones (Princeton Univ. Press, Princeton) (1994)

Propriétés chimiques

• Masse moléculaire: 264.4
• Formule: C₁₇H₂₈O₂
• Couleur/Forme: Neat
• InChI: InChI=1S/C17H28O2/c1-14(2)8-6-9-15(3)10-7-11-16(4)12-13-19-17(5)18/h8,10,12H,6-7,9,11,13H2,1-5H3/b15-10+,16-12+
• Code InChI: InChIKey=ZGIGZINMAOQWLX-NCZFFCEISA-N
• SMILES: CC(=O)OC/C=C(\C)CC/C=C(\C)CCC=C(C)C