13894-62-7

Usage

Uses

Used in Flavor and Fragrance Industry:
METHYLHEX-3-ENOATE is used as a flavoring agent for its fruity, floral aroma, adding a pleasant and natural scent to various food products and beverages. Its unique aroma profile makes it a valuable ingredient in the creation of complex and appealing flavor combinations.
Used in Cosmetics and Personal Care Industry:
METHYLHEX-3-ENOATE is used as a fragrance ingredient in the cosmetics and personal care industry, where it contributes to the overall scent of products such as perfumes, lotions, and shampoos. Its natural, pleasant aroma enhances the sensory experience of these products, making them more appealing to consumers.
Used in the Pharmaceutical Industry:
METHYLHEX-3-ENOATE may also find applications in the pharmaceutical industry, potentially serving as a starting material for the synthesis of various drugs or as an additive in the formulation of medications. Its chemical properties and natural origin make it a promising candidate for further research and development in this field.

InChI:InChI=1/C7H12O2/c1-3-4-5-6-7(8)9-2/h4-5H,3,6H2,1-2H3/b5-4-

Upstream product

• 67-56-1 methanol 
• 504-60-9 penta-1,3-diene 
• 124-38-9 carbon dioxide 
• 87498-17-7 methyl hex-3-ynoate 
• 1918-79-2 2-methylthiophene-5-carboxylic acid 

Downstream Products

• 928-96-1 (Z)-3-Hexen-1-ol 

Relevant academic research and scientific papers

EFFECTIVE HYDROGENATION OF CARBON-CARBON TRIPLE BONDS BY NaBH4/PdCl2 IN POLYETHYLENE GLYCOL/CH2Cl2: USEFULNESS OF PEG IN SYNTHETIC REACTIONS

The NaBH4-PdCl2-polyethylene glycol-CH2Cl2 system has been found to be effective for the hydrogenation of carbon-carbon triple bonds to the corresponding cis-alkenes.

DIENCARBONSAEUREN AUS 1,3-DIENEN UND CO2 DURCH C-C-VERKNUEPFUNG AN NICKEL(0)

(Lig)Ni0 systems react with 1,3-dienes in the presence of CO2 to give nickela carboxylates.The influence of ligands and temperature on the regioselectivity of the C-C bond formation is elucidated.In some cases the nickela carboxylates undergo reductive elimination under the influence of maleic anhydride, and the coupled diene/CO2 moiety rearranges to give the diene carboxylic acid.A possible reaction sequence is discussed.

Lithium/Ammonia Reductions of 2-Thiophenecarboxylic Acids

Lithium/ammonia reductions of 2-thiophenecarboxylic acids (1) in the absence of a proton source afforded mixtures of products.In the presence of methanol acyclic mercapto carboxylic acids (4) were the major products.Ring closure of 4 to the corresponding thiolactones (12) showed the double bonds in 4 to be of cis geometry.Attempts were made to prepare Z olefinic compounds derived from these mercapto carboxylic acids.Lithium 2-thiophenecarboxylate salts (2) afforded good yields of the corresponding 2,5-dihydro-2-thiophenecarboxylic acids (3).The presence of substituents on the ring and the ratio of metal to acid were significant factors in determining the nature of this products.A mechanism is proposed to explain the products observed.

Selective Reactions in Polyethylene Glycol. Hydrogenation of Acetylenes by NaBH4-PdCl2 in Polyethylene Glycol-Methylene Dichloride

The NaBH4-PdCl2-polyethylene glycol-CH2Cl2 system has been found to be effective for the hydrogenation of acetylenic triple bonds to the corresponding cis-alkenes.