100117-62-2

Usage

Uses

Used in Food and Beverage Industry:
ETHYL 3,5-DIMETHYLBENZOYLFORMATE is used as a flavoring agent for its fruity aroma, enhancing the taste and aroma of various food and beverage products.
Used in Perfume and Cosmetic Industry:
ETHYL 3,5-DIMETHYLBENZOYLFORMATE is used as a fragrance ingredient in perfumes and cosmetic products, providing a pleasant and fruity scent to these products.

InChI:InChI=1/C12H14O3/c1-4-15-12(14)11(13)10-6-8(2)5-9(3)7-10/h5-7H,4H2,1-3H3

Upstream product

• 6613-44-1 3,5-dimethylbenzoyl chloride 
• 556-96-7 5-bromo-1,3-xylene 
• 95-92-1 oxalic acid diethyl ester 
• 34696-73-6 3,5-dimethyphenylmagnesium bromide 
• 7647-01-0 hydrogenchloride 
• 99184-68-6 (3,5-dimethyl-phenyl)-glyoxylonitrile 

Downstream Products

• 885058-65-1 hydroxy-(3,5-dimethylphenyl)-acetic acid ethyl ester 
• 1194835-52-3 C₁₀H₉ClO₂ 
• 101277-39-8 cyclohexyl-(3,5-dimethyl-phenyl)-hydroxy-acetic acid 

Relevant academic research and scientific papers

Chiral Frustrated Lewis Pairs Catalyzed Highly Enantioselective Hydrosilylations of 1,2-Dicarbonyl Compounds

A highly enantioselective hydrosilylation of 1,2-dicarbonyl compounds was successfully realized for the first time utilizing the combination of tricyclohexylphosphine and chiral alkenylborane derived in situ from diyne as a frustrated Lewis pair catalyst. A variety of optically active α-hydroxy ketones and esters were obtained in 52-98% yields with 86-99% ee's.

Rhodium(iii)-catalyzed C-H allylation of electron-deficient alkenes with allyl acetates

Rhodium-catalyzed C-H allylation of acrylamides with allyl acetates is reported. The use of weakly coordinating directing group resulted in high reaction efficiency, broad functionality tolerance and excellent γ-selectivity, which opens a new synthetic pathway for the access of 1,4-diene skeletons.

Directing-group-assisted copper-catalyzed olefinic trifluoromethylation of electron-deficient alkenes

Assistance provided: The directing group in the title reaction not only activates the substrates but also allows the stereospecific formation of cis-trifluoromethylated products. The reaction is operationally simple and tolerates a wide variety of functional groups, thus providing an efficient method for the stereoselective synthesis of β-CF3-functionalized acrylamide derivatives. Copyright

Chiral N-heterocyclic carbene ligands for asymmetric catalytic oxindole synthesis

The Pd-catalysed asymmetric intramolecular α-arylation of amide enolates containing heteroatom substituents gives chiral 3-alkoxy or 3-aminooxindoles in high yield and with enantioselectivities up to 97% ee when a new chiral N-heterocyclic carbene ligand is used. The Royal Society of Chemistry.