2648-71-7

Usage

Uses

Used in Pharmaceutical Industry:
3-BROMO-3-METHYL-2-BUTANONE is used as an intermediate in the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 3-BROMO-3-METHYL-2-BUTANONE is utilized as a precursor for the production of agrochemicals, such as pesticides and herbicides. Its reactivity and versatility contribute to the creation of effective and targeted agricultural products.
Used in Fragrance Industry:
3-BROMO-3-METHYL-2-BUTANONE is employed as a building block in the synthesis of various fragrance compounds. Its ability to contribute unique scents and enhance the overall aroma profile of fragrances makes it a valuable component in this industry.
Used as a Reagent in Organic Chemistry:
3-BROMO-3-METHYL-2-BUTANONE is used as a reagent in various organic chemistry reactions, facilitating the synthesis of a wide range of organic compounds. Its reactivity and stability make it a useful tool for chemists in research and development.
Safety Precautions:
Due to its hazardous nature, proper safety precautions should be taken when handling and storing 3-BROMO-3-METHYL-2-BUTANONE. This includes using appropriate personal protective equipment, ensuring proper ventilation, and following established safety guidelines to minimize risks associated with its use.

InChI:InChI=1/C5H9BrO/c1-4(7)5(2,3)6/h1-3H3

Upstream product

• 123-91-1 1,4-dioxane 
• 563-80-4 3-methyl-butan-2-one 
• 60-29-7 diethyl ether 
• 15481-39-7 dioxane dibromide 
• 7789-69-7 phosphorus pentabromide 
• 7726-95-6 bromine 
• 598-75-4 3-methyl-2-butanol 

Downstream Products

• 7333-23-5 2,2,6-trimethyl-3,5-heptanedione 
• 115-22-0 3-Hydroxy-3-methyl-2-butanone 
• 2442-13-9 3,3-dimethoxy-2-methyl-butan-2-ol 
• 598-98-1 Methyl pivalate 
• 799827-17-1 3,3-diethoxy-2-methyl-butan-2-ol 
• 3938-95-2 2,2-dimethyl-propanoic acid ethyl ester 
• 35875-02-6 2-methyl-2-phenylsulfanylbutan-3-one 
• 62291-77-4 3-benzenesulfonyl-3-methyl-butan-2-one 
• 42855-44-7 3-mercapto-3-methyl-butan-2-one 
• 1518-06-5 1,3-dibromo-3-methyl-2-butanone 
• 770-85-4 2-methyl-2-phenylbutan-3-one 
• 75-98-9 Trimethylacetic acid 
• 69278-36-0 3-bromo-3-methyl-2-trimethylsiloxy-1-butene 
• 37719-02-1 2,2-dimethyl-3-oxobutanenitrile 

Relevant academic research and scientific papers

Fast oxidation of secondary alcohols by the bromate-bromide system using cyclic microwave heating in acidic water

We report an improved, gentle, cyclic microwave activation technique for the oxidation of secondary alcohols using nonhazardous hypobromous acid (BrOH) as the reagent in acidic water. Several aliphatic and aromatic secondary alcohols were successfully oxidized to the corresponding ketones using this technique in high yields and with only minor amounts of side products.

A mild and efficient procedure for α-bromination of ketones using N-bromosuccinimide catalysed by ammonium acetate

Cyclic ketones reacted with N-bromosuccinimide (NBS) catalysed by NH 4OAc in Et2O at 25°C to give the corresponding α-brominated ketones in good yields, while acyclic ketones were efficiently brominated in CCl4 at 80°C.

PREPARATION OF vic-MERCAPTOISOPENTANOLS

This paper describes the preparation of some mercaptoisopentanols: 2-mercapto-3-methyl-1-butanol (I), 1-mercapto-3-methyl-2-butanol (II), 3-mercapto-3-methyl-2-butanol (III) and the unsaturated analogue of compound I - 2-mercapto-3-methyl-2-buten-1-ol (IV).These compounds belong to the flavonoid group present in food responsible for deterioration of their gustatory properties.

Natural Product Chemistry. Part 116. Synthesis of Daurine and Folidine: Two 2(1H)-Quinolinone Alkaloids from Haplophyllum Species

Structures of the recently isolated 2(1H)-quinolinone alkaloids, daurine and folidine have been confirmed by total synthesis. - Keywords: Alkaloids; Daurine; Folidine; Haplophyllum; 2(1H)-Quinolinones; Rutaceae; Total synthesis