6138-88-1

Usage

Uses

Used in the Food Industry:
1-(3-Methyl-2-furanyl)-3-methyl-2-buten-1-one is used as a flavoring ingredient for its sweet, fruity aroma, enhancing the taste and smell of various food products.
Used in the Perfume and Fragrance Industry:
1-(3-Methyl-2-furanyl)-3-methyl-2-buten-1-one is utilized as a key component in the production of perfumes and fragrances, capitalizing on its pleasant and appealing scent to create captivating scents for consumer products.
Used in Pharmaceutical Research:
1-(3-Methyl-2-furanyl)-3-methyl-2-buten-1-one is studied for its potential pharmacological properties, including antibacterial and antifungal activities, indicating its possible use in the development of new medicines and treatments.

Upstream product

• 78173-38-3 3-Methyl-1-(3-methyl-furan-2-yl)-but-3-en-1-one 
• 78173-37-2 3-Chloro-3-methyl-1-(3-methyl-furan-2-yl)-butan-1-one 
• 22601-06-5 3-methylfuran-2-carbonyl chloride 
• 71478-44-9 2-methyl-1-propenylmanganese chloride 
• 109603-93-2 C₄H₇BrMn 
• 62485-91-0 iodo-(2-methyl-propenyl)-manganese 
• 18292-39-2 (2-methyl-1-propen-1-yl)trimethylsilane 

Downstream Products

• 488-05-1 3-methyl-1-(3-methylfuran-2-yl)butan-1-one 
• 93016-60-5 3-methyl-1-(3-methyl-[2]furyl)-but-2-en-1-one-((Z)-2,4-dinitro-phenylhydrazone) 
• 93016-60-5 3-methyl-1-(3-methyl-[2]furyl)-but-2-en-1-one-((E)-2,4-dinitro-phenylhydrazone) 

Relevant academic research and scientific papers

Wittig rearrangement of 3-furylmethyl ethers: Facile synthesis of 3-metyl-2-furylmethanols and 3-furylethanols

Wittig rearrangement of 3-furylmethyl ethers 1a-i was investigated. Deprotonation of 3-furylmethyl ethers 1a-i with bases, such as BuLi and LDA, occurred preferentially at the allylic, propargylic, benzylic positions and α-position adjacent to carbonyl gr

A new simple route to furanic ketones; preparation of elsholtzione naginata ketone and perilla ketone

Copper- or iron-catalyzed acylation of organomanganese reagents allows to obtain 3- and 2-acylfurans in high yields. Elsholtzione, naginata ketone and perilla ketone have been prepared according to this procedure.

A NEW AND SHORT SYNTHESIS OF DEHYDROELSHOLTZIONE (NAGINATA KETONE) AND ISOEGOMAKETON

1-Trimethylsilyl 2-methyl 1-propene and 1-trimethylsilyl 3-methyl 1-butene are useful intermediates for the synthesis of furan natural compounds such as Naginata ketone and isoegomaketone.