58334-55-7

Basic information

• Product Name: zingiberenol
• Synonyms: zingiberenol;1,10-Bisaboladien-3-ol;4-(1,5-Dimethyl-4-hexenyl)-1-methyl-2-cyclohexen-1-ol
• CAS NO: 58334-55-7
• Molecular Formula: C₁₅H₂₆O
• Molecular Weight: 222.37
• Mol File: 58334-55-7.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 304.1±21.0 °C(Predicted)
• Appearance: /
• Density: 0.914±0.06 g/cm3(Predicted)
• PKA: 14.75±0.40(Predicted)
• CAS DataBase Reference: zingiberenol(CAS DataBase Reference)
• NIST Chemistry Reference: zingiberenol(58334-55-7)
• EPA Substance Registry System: zingiberenol(58334-55-7)

Safety Data

• Hazardous Substances Data: 58334-55-7(Hazardous Substances Data)

Usage

General Description

Zingiberenol is a bioactive compound found in ginger plants that has been shown to possess various pharmacological properties. It has been identified as a potent anti-inflammatory agent, with studies demonstrating its ability to reduce inflammation by inhibiting the production of pro-inflammatory mediators. Zingiberenol also exhibits antioxidant properties, helping to protect cells from oxidative stress and damage. In addition, this chemical has been studied for its potential anti-cancer effects, showing promise in inhibiting the growth of cancer cells and inducing apoptosis. Overall, zingiberenol appears to be a valuable compound with potential therapeutic applications in treating inflammatory conditions, oxidative stress-related diseases, and cancer.

Upstream product

• 917-64-6 methyl magnesium iodide 
• 1723-80-4 4-(6-methyl-5-hepten-2-yl)-2-cyclohexen-1-one 
• 4434-77-9 2-bromo-6-methylhept-5-ene 
• 93158-30-6 6.10-Dimethyl-2-oxo-undec-9-en-5-carbonsaeure-aethylester 
• 94435-68-4 Diethyl-6,10-dimethyl-2-oxo-undec-9-en-5,5-dicarboxylat 
• 56422-95-8 ethyl-2-carbethoxy-3,7-dimethyl-oct-6-enoate 
• 917-54-4 methyllithium 
• 106-23-0 3,7-dimethyl-oct-6-enal 
• 22418-66-2 3,7-dimethyl-2-methyleneoct-6-enal 
• 4582-61-0 2-<(tolylsulfonyl)oxy>-6-methyl-5-heptene 
• 100572-83-6 4-(1,5-dimethyl-4-hexenyl)-3-cyclohexen-1-one 
• 81841-89-6 4,4-(ethylenedioxy)-1-(phenylsulfonyl)cyclohexene 
• 344903-14-6 8-Benzenesulfonyl-8-(1,5-dimethyl-hex-4-enyl)-1,4-dioxa-spiro[4.5]dec-6-ene 
• 110-93-0 6-Methyl-hept-5-en-2-on 

Downstream Products

• 38738-45-3 racemic zingiberene 
• 1030630-94-4 4-[3-(3,3-dimethyloxiran-2-yl)-1-methylpropyl]-1-methylcyclohex-2-en-1-ol 

Relevant articles and documents

MURGANTIOL AS A STINK BUG SYNERGISTIC ATTRACTANT FOR USE OUTDOORS

Provided herein are uses of the Harlequin bug pheromone, murgantiol, alone or in a synergistic combination with at least one other stink bug attractant, such as methyl (2E,4E,6Z)-decatrienoate or methyl (2E,4Z)-decadienoate, or both, for attracting stink bugs such as the brown marmorated stink bug in outdoor settings. Stink bug traps comprising murgantiol, or synergistic compositions comprising murgantiol with at least one other stink bug attractant, and methods of using these compositions in traps outdoors are provided. Compositions comprising murgantiol are also described as synergistic combinations of murgantiol with at least one other stink bug attractant.

Regiocontrolled Synthesis of Mono-, Di, and Trisubstituted Cyclohexenones by Cycloaddition of Vinyl Sulfones to 1-Methoxy-3--1,3-butadienes. Conversion of Alkenes into Effective Dienophilic Reagents

Cycloaddition of phenyl vinyl sulfone to Danishefky's diene followed by direct ketalization provided 7, a synthon for the 4-(2-cyclohexenyl) anion.Thus, 7 readily undergoes regiospecific γ-alkylation.Ensuing reductive desulfonylation and hydrolysis provides 2-(and 3-)-cyclohexenones efficiently.Zingiberenol, a monocyclic sesquiterpene, was prepared by means of this methodology.Terminal alkenes and cyclic olefins enter into comparable regiocontrolled Diels-Alder addition if they are first subjected to selenosulfonation and oxidation to the vinyl sulfone.Removal of the phenylsulfonyl substituent after condensation provides the adducts which are formally derived from alkylation of the hypothetical C5 anion of 2-cyclohexenone.The scheme can be expanded to include γ-alkylation prior to desulfonylation.By this means, one is able to prepare 4,5-disubstituted 2-(and 3-)cyclohexenones where the nature of the pendant side chains can be widely varied.