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Usage

Uses

Used in Flavoring and Fragrance Industry:
(S)-3-METHYLHEXANOIC ACID is used as a flavoring agent for its fruity and cheesy odor, enhancing the aroma profiles in various food products and contributing to the creation of unique scents in perfumes and other fragrances.
Used in Pharmaceutical Industry:
(S)-3-METHYLHEXANOIC ACID is used as a precursor in the synthesis of other organic compounds, playing a crucial role in the development of pharmaceutical products due to its unique structural properties.
Used in Cosmetics Industry:
(S)-3-METHYLHEXANOIC ACID is used as an ingredient in cosmetic formulations, leveraging its unique properties to contribute to the texture, stability, or scent of the final product.
Used in Chemical Synthesis:
(S)-3-METHYLHEXANOIC ACID is used as a building block in the synthesis of a variety of organic compounds, showcasing its versatility and importance in the chemical industry.

Upstream product

• 96864-25-4 (R)-3-Methyl-hexanoic acid (1S,2R,4R)-1-[(dicyclohexylsulfamoyl)-methyl]-7,7-dimethyl-bicyclo[2.2.1]hept-2-yl ester 
• 26184-62-3 (S)-2-pentanol 
• 104897-87-2 (S)-3-Methyl-hexanoic acid (1S,2R,4R)-1-[(dicyclohexylsulfamoyl)-methyl]-7,7-dimethyl-bicyclo[2.2.1]hept-2-yl ester 

Downstream Products

• 86423-92-9 (3R)-3-Methylhexan-1-ol 
• 188123-53-7 (1S,2R,6S,7S,8S)-8-(tert-Butyl-diphenyl-silanyloxy)-5-((S)-3-methyl-hexanoyl)-3-oxa-5-aza-tricyclo[5.2.1.0^2,6]decan-4-one 
• 13231-81-7 (3S)-3-Methylhexan-1-ol 
• 65530-93-0 (-)(S)-1-amino-3-methyl-hexane 
• 53783-89-4 (+)(S)-3-methyl-caproic acid nitrile 
• 101257-63-0 (+)(S)-1-chloro-3-methyl-hexane 

Relevant academic research and scientific papers

Method for the Production of Optically Active 3-Alkyl Carboxylic Acids and the Intermediate Products Thereof

An enantioselective method for producing optically active 3-alkyl carboxylic acids comprises transforming an optically active secondary alcohol into an optically active, activated compound by introducing a leaving group; reacting the activated compound with a malonic acid derivative to obtain an optically active, alkylated malonic acid compound, the reaction taking place exclusively in ether and/or carboxylic acid ester solvents and one or more aprotic polar solvents or alcohols as a cosolvent in a maximum proportion of 30 volume percent of total solvent, wherein the added cosolvent is not hexamethyl phosphoric acid triamide; the malonic acid compound is hydrolyzed if necessary to obtain the corresponding acid; and the corresponding acid is decarboxylated.

Camphorsulfonamide-Shielded, Asymmetric 1,4-Additions and Enolate Alkylations; Synthesis of a Southern Corn Rootworm Pheromone

Using readily accessible 10-sulfonamido-isoborneols as regenerable, chiral auxiliaries, highly face-selective C-C-bond formations at Cα and Cβ of carboxylates could be conveniently achieved.Thus, conjugated additions of RCu to enoates (1->2) furnished, after saponification, β-substituted carboxylic acids 3 in 94-98 percent e.e.Similarly, propionates 12 yielded after deprotonation, enolate alkylation, and reductive ester cleveage the (R)-alcohols 15 in 78-98 percent e.e.The acid (+)-3e was converted to the pheromone (-)-11.