2520-57-2

Basic information

• Product Name: Bis(4-methyl-3-pentenyl) ketone
• Synonyms: 2,10-Dimethyl-2,9-undecadien-6-one;Bis(4-methyl-3-pentenyl) ketone
• CAS NO: 2520-57-2
• Molecular Formula: C13H22O
• Molecular Weight: 194.31
• Mol File: 2520-57-2.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Bis(4-methyl-3-pentenyl) ketone(CAS DataBase Reference)
• NIST Chemistry Reference: Bis(4-methyl-3-pentenyl) ketone(2520-57-2)
• EPA Substance Registry System: Bis(4-methyl-3-pentenyl) ketone(2520-57-2)

Safety Data

• Hazardous Substances Data: 2520-57-2(Hazardous Substances Data)

Upstream product

• 6407-36-9 N-isopropyliden-cyclohexyl amine 
• 870-63-3 prenyl bromide 
• 153078-07-0 7-Methyl-2-(3-methyl-but-2-enyl)-3-oxo-oct-6-enoic acid methyl ester 
• 110-93-0 6-Methyl-hept-5-en-2-on 
• 53067-23-5 methyl 7-methyl-3-oxooct-6-enoate 
• 1040738-23-5 2-fluoro-6-((2-methylbut-3-en-2-yl)oxy)pyridine 
• 1040738-62-2 C₁₁H₁₈O₂S₂ 

Relevant articles and documents

Preparation of the Hexanolide Isolated from Conyza hypoleuca

A synthesis of racemic 13-hydroxy-10-sesquigeranic-1,12-olide is reported using bis(sym-collidine)iodine(I) hexafluorophosphate in the lactonisation key step.

Allylic alcohols as radical allylating agents. An overall olefination of aldehydes and ketones

2-Fluoropyridyl derivatives of allylic alcohols react with xanthates in the presence of lauroyl peroxide to give alkenes, often with high stereoselectivity. If the allylic alcohols are themselves derived from aldehydes or ketones, the overall process becomes a synthetic equivalent of the classical Wittig and related olefination reactions. Copyright