106536-22-5

Basic information

• Product Name: 3,3-bis(3-phenyl-2-propen-1-yl)pentane-2,4-dione
• Synonyms: 3,3-bis(3-phenyl-2-propen-1-yl)pentane-2,4-dione
• CAS NO: 106536-22-5
• Molecular Weight: 332.442
• Mol File: 106536-22-5.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 3,3-bis(3-phenyl-2-propen-1-yl)pentane-2,4-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 3,3-bis(3-phenyl-2-propen-1-yl)pentane-2,4-dione(106536-22-5)
• EPA Substance Registry System: 3,3-bis(3-phenyl-2-propen-1-yl)pentane-2,4-dione(106536-22-5)

Safety Data

• Hazardous Substances Data: 106536-22-5(Hazardous Substances Data)

Upstream product

• 98-03-3 thiophene-2-carbaldehyde 
• 4407-36-7 (2E)-3-phenyl-2-propen-1-ol 
• 104-55-2 3-phenyl-propenal 
• 4392-24-9 Cinnamyl bromide 
• 123-54-6 acetylacetone 
• 110-89-4 piperidine 
• 4393-06-0 1-Phenyl-2-propen-1-ol 
• 14321-27-8 N-ethylbenzylamine 
• 21040-45-9 Cinnamyl acetate 
• 104-88-1 4-chlorobenzaldehyde 
• 513-42-8 3-hydroxy-2-methyl-1-propene 
• 500-22-1 3-pyridinecarboxaldehyde 
• 541-57-1 4-hydroxy-2(5H)-furanone 

Relevant articles and documents

Solvent-controlled highly selective bis-and monoallylation of active methylene compounds by allyl acetate with palladium(0) nanoparticle

(Chemical Equation Presented) Palladium(0) nanoparticle has been used as an efficient catalyst for the allylation of active methylene compounds. Very efficient bisallylation is achieved for a variety of active methylene compounds by allyl acetate and its derivatives in one stroke in THF solvent. The reaction in water provides monoallylated product selectively by allyl acetate only. The recovered Pd(0) nanoparticle is recycled. A probable mechanism is suggested.

Solvent-free synthesis of 4,4-bis-functionalized-1,6-dienes and 1,6-diynes on the surface of neutral alumina

An improved procedure has been developed for the synthesis of structurally varied 4,4-bis-functionalized-1,6-dienes and 1,6-diynes through regioselective alkylation of active methylene compounds with several unsymmetrical allyl bromides and propargyl brom

Micellar catalysis using a photochromic surfactant: Application to the pd-catalyzed tsuji-trost reaction in water

The first example of a Pd-catalyzed Tsuji-Trost reaction, applied in a photochromic micellar media under conventional heating and microwave irradiation, is reported. The surfactant activity and recycling ability were investigated and compared with those of a few commercially available surfactants. The synthetic photochromic surfactant proved to be efficient, recyclable, and versatile for Pdcatalyzed coupling reactions.