7147-33-3

Usage

Uses

Used in Perfumery Industry:
ETHYL A-ETHOXYOXALYLPHENYL ACETATE is used as a fragrance ingredient for its sweet, floral scent, contributing to the creation of various perfumes.
Used in Soap Industry:
In the soap industry, ETHYL A-ETHOXYOXALYLPHENYL ACETATE is used as a flavoring agent to impart a pleasant aroma to soaps and other cleaning products.
Used in Cosmetics Industry:
ETHYL A-ETHOXYOXALYLPHENYL ACETATE serves as a fragrance component in cosmetics, enhancing the sensory experience of these products.
Used in Other Scented Products:
Beyond the primary industries, ETHYL A-ETHOXYOXALYLPHENYL ACETATE is also utilized in other products that require a pleasant scent, such as candles, air fresheners, and personal care items.

InChI:InChI=1/C14H16O5/c1-3-18-13(16)11(10-8-6-5-7-9-10)12(15)14(17)19-4-2/h5-9,11H,3-4H2,1-2H3

Upstream product

• 101-97-3 Ethyl 2-phenylethanoate 
• 95-92-1 oxalic acid diethyl ester 
• 60-29-7 diethyl ether 
• 140-29-4 phenylacetonitrile 
• 119174-42-4 2-ethoxy-2-oxoacetic anhydride 

Downstream Products

• 22286-82-4 2-phenyl-acrylic acid ethyl ester 
• 63285-97-2 2-methyl-5-oxo-4-phenyl-2,5-dihydro-isoxazole-3-carboxylic acid ethyl ester 
• 83-13-6 diethyl 2-phenylmalonate 
• 1309477-15-3 C₃₁H₃₄N₂O₂ 
• 1309477-17-5 C₃₃H₃₈N₂O₂ 
• 1309477-19-7 C₃₅H₄₂N₂O₂ 
• 1309477-21-1 C₃₇H₄₆N₂O₂ 
• 1309477-23-3 C₃₉H₅₀N₂O₂ 
• 37818-48-7 2-Phenyl-propanedioyl dichloride 
• 59530-33-5 dipentachlorophenyl phenylmalonate 
• 56431-38-0 3,6-Dihydro-1,2,3,5-tetraphenyl-1-pyrimidinium-4-olat 

Relevant academic research and scientific papers

Asymmetric Synthesis of Spiropyrazolones by Rhodium-Catalyzed C(sp2)?H Functionalization/Annulation Reactions

Rhodium-catalyzed C(sp2)?H functionalization reactions of 4-aryl-5-pyrazolones followed by [3+2] annulation reactions with alkynes provide rapid access to highly enantioenriched five-membered-ring 4-spiro-5-pyrazolones. The use of a chiral SCpRh catalyst enabled the synthesis of a large range of spiropyrazolones with all-carbon quaternary stereogenic centers in up to 99 % yield and 98 % ee from readily available substrates.

Total synthesis of monocyclic pyrimidinium betaines with fatty alkyl chains

Seven betaines were prepared by condensation of N,N'-diphenylamidines with malonic acid derivatives. The amidines were made via a multistep synthesis, starting from their corresponding fatty acids. Malonyl chloride and dipentachlorophenyl phenylmalonate, two derivatives of malonic acid, were obtained from malonic acid and benzyl chloride, respectively. Most of the products were characterized by IR, UV, 1H and 13C NMR. Biological assays of the synthesized betaines revealed their good antibacterial and antifungal activities against the Pseudomonas aeruginosa, Bacillus subtilis and Mucor ramannianus and an activity against Candida albicans.

Studies on non-thiazolidinedione antidiabetic agents. 1. Discovery of novel oxyiminoacetic acid derivatives

A novel series of oxyiminoacetic acid derivatives were synthesized in an effort to develop a potent antidiabetic agent, which does not contain the 2,4-thiazolidinedione moiety. These compounds were evaluated for glucose and lipid lowering effects in genetically obese and diabetic KKAy mice. Several of the compounds showed strong antidiabetic activity, including functional potency at peroxisome proliferator-activated receptor (PPAR)-γ. (Z)-2-[4-[(5-Methyl-2-phenyl-1,3-oxazol-4-yl)methoxy]benzyloxyimino]-2-(4- phenoxyphenyl)acetic acid (25) significantly reduced plasma glucose (33%, p0.01) and plasma triglycelide levels (43%, p0.01) even at a dosage of 0.001% in diet. Pharmacokinetic analyses of 25 are also reported.

Disposition of bornaprine hydrochloride in the rat. 1st Communication: Pharmacokinetic studies: Synthesis, plasma levels and elimination

The biliary elimination and plasma concentration-time course of radioactivity and unchanged compound of 2-phenyl-bicyclo-[2.2.1]-heptane-2-carboxylic acid (4'-diethylaminopropyl)ester hydrochloride (bornaprine hydrochloride, Sormodren) were investigated a

Intramolecular Carbenoid Reactions of Pyrrole Derivatives. A Total Synthesis of (+/-)-Ipalbidine

A mew method for alkaloid synthesis is described.The rhodium(II)-acetate-catalyzed decomposition of 3-(4-acetoxyphenyl)-1-diazo-4-(pyrrol-1-yl)-2-butanone (5d) gave 6-(4-acetoxyphenyl)-5,6-dihydro-7(8H)-indolizinone (6d) in 82percent yield via an intramolecular carbenoid reaction.The latter compound was converted in four steps in 13percent overall yield to (+/-)-ipalbidine (1b).

COMPETITIVE INTRAMOLECULAR CARBENOID REACTIONS OF PYRROLE DERIVATIVES

Rhodium(II) acetate-catalyzed decomposition of 1-diazo-3-phenyl-4-(pyrrol-1-yl)-butan-2-one and its p-methoxy derivative resulted in their intramolecular cyclization to form the 6-phenyl-5,6-dihydroindolizin-7(8H)-ones and 1-(pyrrol-1-yl)methylindan-3-ones as major and minor products respectively in high yields (77-89percent).The p-nitrophenyldiazo compound cyclized exclusively to the 5,6-dihydroindolizin-7(8H)-one in 76percent yield.