17404-06-7

Basic information

• Product Name: (E)-2-(4-methoxyphenyl)pent-2-ene
• Synonyms: (E)-2-(4-methoxyphenyl)pent-2-ene
• CAS NO: 17404-06-7
• Molecular Weight: 176.258
• Mol File: 17404-06-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (E)-2-(4-methoxyphenyl)pent-2-ene(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-2-(4-methoxyphenyl)pent-2-ene(17404-06-7)
• EPA Substance Registry System: (E)-2-(4-methoxyphenyl)pent-2-ene(17404-06-7)

Safety Data

• Hazardous Substances Data: 17404-06-7(Hazardous Substances Data)

Upstream product

• 829-17-4 1‐(1‐cyclopropylvinyl)‐4‐methoxybenzene 
• 1393706-26-7 (E)-1-(5-bromopent-2-en-2-yl)-4-methoxybenzene 
• 91763-97-2 2-(4-Methoxy-phenyl)-pentanol-⁽²⁾ 
• 927-77-5 n-propylmagnesium bromide 
• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 7152-03-6 p-methoxyphenyl cyclopropyl ketone 

Downstream Products

• 1373368-64-9 2-(4-methoxyphenyl)pent-1-en-3-one 
• 4097-42-1 2-<4-Hydroxy-3,5-dinitro-phenyl>-pentan 
• 94-06-4 2-(4-Hydroxyphenyl)pentane 
• 4125-32-0 4-(1-methyl-butyl)-anisole 

Relevant articles and documents

Direct Synthesis of Enones by Visible-Light-Promoted Oxygenation of Trisubstituted Olefins Using Molecular Oxygen

A one-step synthesis of enones from olefins is described. The reaction was performed under visible-light irradiation in the presence of molecular oxygen and a photocatalyst. The reaction proceeded with various types of trisubstituted olefins to give enones in good yields with high regioselectivity. In particular, oxygen- and nitrogen-containing functional groups, heteroaromatic rings, and cyclopropanes were tolerated. Mechanistic studies and previous reports indicated that the active oxygen species generated in the reaction system is singlet oxygen.

Structures and pesticidal activities of derivatives of dinitro-phenols. IV. Preparation of certain 2-(alpha-branched alkyl)-4,6-dinitro- and 4-(alpha-branched alkyl)-2,6-dinitro-phenols.

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