114727-96-7

Basic information

• Product Name: FERPRENIN
• Synonyms: FERPRENIN;(+)-2-[(E)-4,8-Dimethyl-3,7-nonadienyl]-2-methyl-2H,5H-pyrano[3,2-c][1]benzopyran-5-one;2-[(E)-4,8-Dimethyl-3,7-nonadienyl]-2-methyl-2H,5H-pyrano[3,2-c][1]benzopyran-5-one
• CAS NO: 114727-96-7
• Molecular Formula: C24H28 O3
• Molecular Weight: 0
• Mol File: 114727-96-7.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: FERPRENIN(CAS DataBase Reference)
• NIST Chemistry Reference: FERPRENIN(114727-96-7)
• EPA Substance Registry System: FERPRENIN(114727-96-7)

Safety Data

• Hazardous Substances Data: 114727-96-7(Hazardous Substances Data)

Upstream product

• 1076-38-6 4-hydroxy[1]benzopyran-2-one 
• 502-67-0 Farnesal 
• 6805-34-1 E,E-3-farnesyl-4-hydroxycoumarin 

Relevant articles and documents

FERPRENIN, A PRENYLATED COUMARIN FROM FERULA COMMUNIS

Key Word Index-Ferula communis; Umbelliferae; prenylated coumarins; ferprenin; ferulenol.The structure of ferprenin, a prenylated coumarin from Ferula communis, has been established from spectral data, and by synthesis from E,E-farnesal and 4-hydroxycoumarin.Ferprenin could also be obtained from ferulenol, the major constituent of the plant investigated, by a Cr(6+)-mediated oxidative cyclization, for which a possible mechanism is proposed.

Green one-pot synthesis of 2h-pyrans under solvent-free conditions catalyzed by ethylenediammonium diacetate

Ethylenediammonium diacetate readily catalyzes the Knoevenagel-type condensation between 1,3-dicarbonyl substrates and ,-unsaturated aldehydes at room temperature under solvent-free conditions. This rapid, efficient, and convenient one-pot approach to the

Environmentally benign, one-pot synthesis of pyrans by domino Knoevenagel/6π-electrocyclization in water and application to natural products

In water medium, environmentally benign, facile, and efficient synthesis of pyrans was achieved in good yields by the reactions of a variety of cyclic 1,3-dicarbonyls with several α,β-unsaturated aldehydes. The key strategy was a formal [3+3] cycloaddition by domino Knoevenagel/6π- electrocyclization. This methodology was applied to the synthesis of biologically interesting pyranocoumarin, pyranoquinolinone, and pyranonaphthoquinone derivatives along with selected natural and non-natural products. The Royal Society of Chemistry 2010.