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Usage

Uses

Used in Fragrance and Flavoring Industry:
2,5-Cyclohexadien-1-one, 2,6-bis(1,1-dimethylethyl)-4-methyl-4-(2-propenyl)is used as a key component in the production of fragrances and flavorings due to its distinctive and appealing scent. It contributes to the creation of various scents and tastes in a wide range of consumer products, including perfumes, colognes, and food items.
Used in Organic Synthesis:
In the field of organic synthesis, 2,5-Cyclohexadien-1-one, 2,6-bis(1,1-dimethylethyl)-4-methyl-4-(2-propenyl)serves as a valuable intermediate for the synthesis of other organic compounds. Its unique structure allows it to be a versatile building block in the development of new chemical entities for various applications, such as pharmaceuticals, agrochemicals, and specialty chemicals.
Safety Considerations:
Given its flammability and potential health hazards, 2,5-Cyclohexadien-1-one, 2,6-bis(1,1-dimethylethyl)-4-methyl-4-(2-propenyl)should be handled with care in industrial settings. Proper safety measures, including the use of protective equipment and adherence to safety protocols, are essential to minimize risks associated with its use.

Upstream product

• 128-37-0 2,6-di-tert-butyl-4-methyl-phenol 
• 762-72-1 allyl-trimethyl-silane 
• 107-05-1 3-chloroprop-1-ene 

Downstream Products

• 37723-24-3 2,6-Di-tert-butyl-p-tolylphenylsulfid 
• 37723-23-2 4-(3-Butenyl)-3,5-di-tert-butyltoluol 
• 34712-56-6 4-Allyl-2,6-di-tert-butyl-4-methyl-1-phenyl-cyclohexa-2,5-dienol 
• 37723-20-9 (3,5-Di-tert-butyl-1-methyl-4-oxo-cyclohexa-2,5-dienyl)-acetaldehyde 
• 34918-82-6 3-Allyl-1,5-di-tert-butyl-3-methyl-6-methylene-cyclohexa-1,4-diene 
• 37723-19-6 2,6-Di-tert-butyl-4-cyclopropylmethyl-4-methyl-cyclohexa-2,5-dienone 

Relevant academic research and scientific papers

Investigating the microwave-accelerated Claisen rearrangement of allyl aryl ethers: Scope of the catalysts, solvents, temperatures, and substrates

The microwave-accelerated Claisen rearrangement of allyl aryl ethers was investigated, in order to gain insight into the scope of the catalysts, solvents, temperatures, and substrates. Among the catalysts examined, phosphomolybdic acid (PMA) was found to greatly accelerate the reaction in NMP, at temperatures ranging from 220 to 300 °C. This method was found to be useful for preparing several intermediates previously reported in the literature using precious metal catalysts such as Au(I), Ag(I), and Pt(II). Additionally, substrates bearing bromo and nitro groups on the aryl portion required careful tailoring of the reaction conditions to avoid complex product profiles.

'Aromatic ring umpolung', a rapid access to the main core of several natural products

Treatment of various substituted phenols in the presence of (diacetoxyiodo)benzene promotes the formation of a phenoxenium ion, a very electrophilic species able to react with various nucleophiles leading rapidly to a plethora of different cores present i

On the way to an oxidative Hosomi-Sakurai reaction

An oxidative allylation process mediated by a hypervalent iodine reagent has been performed on polysubstituted phenols. This reaction, occurring in useful to good yields, leads to a rapid access to dienones containing a quaternary carbon center. Georg Thieme Verlag Stuttgart.