18641-70-8

Usage

Uses

Used in Industrial Processes:
2,4-Dimethyl-3-hexanone is used as a solvent for its ability to dissolve a wide range of substances, making it indispensable in various manufacturing and processing applications.
Used in Chemical Production:
In the chemical industry, 2,4-dimethyl-3-hexanone is used as a key component in the production of insecticides, herbicides, and pharmaceuticals, contributing to the effectiveness and formulation of these products.
Used in Organic Synthesis:
2,4-Dimethyl-3-hexanone serves as a valuable intermediate in organic synthesis, facilitating the creation of complex molecules and compounds for research and commercial purposes.
Used in the Food Industry:
As a flavoring agent, 2,4-dimethyl-3-hexanone is employed to enhance the taste and aroma of food products, ensuring a more appealing sensory experience for consumers.

InChI:InChI=1/C8H16O/c1-5-7(4)8(9)6(2)3/h6-7H,5H2,1-4H3/t7-/m0/s1

Upstream product

• 13432-25-2 2,4-dimethyl-hexan-3-ol 
• 671795-46-3 sec-butylmagnesium bromide 
• 79-30-1 isobutyryl chloride 
• 5856-79-1 iso-butyl chloroformate 
• 1068-55-9 isopropylmagnesium chloride 
• 116-53-0 2-Methylbutanoic acid 
• 136840-13-6 4-acetoxy-2,4-dimethyl-1-penten-3-one 
• 136839-81-1 4-bromo-2,4-dimethyl-1-penten-3-one 
• 21980-74-5 2-bromo-4-hydroxy-2,4-dimethyl-pentan-3-one 
• 15185-08-7 4-hydroxy-2,4-dimethylpent-1-en-3-one 
• 17346-16-6 2,4-dibromo-2,4-dimethylpentan-3-one 
• 3212-67-7 2-hydroxy-3-oxo-2,4-dimethyl-pentane 
• 3212-63-3 2-bromo-2,4-dimethyl-3-pentanone 
• 67-56-1 methanol 

Downstream Products

• 13432-25-2 2,4-dimethyl-hexan-3-ol 
• 14255-23-3 2,4-dimethylhex-2-ene 
• 205485-97-8 2,2,3-Trimethyl-1-isopropyl-1-cyclopropylthiol 
• 20739-54-2 2,4-Dimethyl-3-phenyl-hexan-3-ol 

Relevant academic research and scientific papers

Catalytic synthesis of oxygenate from alcohol

The present invention discloses a method for catalytic synthesis of oxygenate from alcohol. At first, a feeding material comprising at least one alcohol is provided. Next, a copper-containing catalyst is provided and the catalyst further comprises at least one metal element selected from the group consisting of the following: zinc, magnesium, and aluminum elements. Following that, a catalytic reaction of the feeding material over the copper-containing catalyst is carried out to synthesize at least one oxygenate.

Functional Group Hybrids. Reactivity of α'-Nucleofuge α,β-Unsaturated Ketones. 1. Reactions with Organocopper Reagents

A series of α-nucleofuge α',β'-unsaturated ketones encompassing a variety of structural types and nucleofuges was prepared.Treatment of these compounds with lithium dimethylcuprate or methylcopper leads primarily to either reductive cleavage of the α-nucl

CONDENSATION DES ORGANOMAGNESIENS SUR LES CHLORUSES D'ACIDE DANS LE TETRAHYDROFURANNE A BASSE TEMPERATURE

The condensation of a Grignard reagents with hindered acid chlorides in THF at low temperature, yields ketones which are generally difficult to obtain and avoids the side reaction caused with a CuCl catalyst.Applied to unsaturated Grignard reagents and acid chlorides, this method also yields unsaturated ketones, such as the Artemisia ketone.