6975-15-1

Usage

Uses

Used in Flavor and Fragrance Industry:
1-Oxaspiro[2.4]heptane-2-carboxylic acid, ethyl ester is used as a flavoring agent for its sweet, fruity scent, enhancing the taste and aroma of various food and beverage products.
Used in Perfumery:
In the perfume industry, 1-Oxaspiro[2.4]heptane-2-carboxylic acid, ethyl ester is used as a fragrance ingredient to add a pleasant, fruity note to perfumes, contributing to the overall scent profile.
Used in Cosmetics and Soaps:
This ester is also utilized in cosmetics and soaps as a fragrance component, providing a fresh and appealing scent to these personal care products.
Used in Organic Synthesis:
1-Oxaspiro[2.4]heptane-2-carboxylic acid, ethyl ester is employed as a building block in the synthesis of other organic compounds, contributing to the creation of a wide range of chemical products.
Used as a Solvent in Chemical Processes:
In various chemical processes, this ester serves as a solvent, facilitating reactions and aiding in the dissolution of other substances.
It is crucial to handle 1-Oxaspiro[2.4]heptane-2-carboxylic acid, ethyl ester with care due to its potential to cause skin and eye irritation, and its harmful effects if ingested or inhaled.

InChI:InChI=1/C9H14O3/c1-2-11-8(10)7-9(12-7)5-3-4-6-9/h7H,2-6H2,1H3

Upstream product

• 141-52-6 sodium ethanolate 
• 105-39-5 chloroacetic acid ethyl ester 
• 120-92-3 cyclopentanone 
• 105-36-2 ethyl bromoacetate 

Downstream Products

• 33537-18-7 cyclopentyl-oxo-acetic acid ethyl ester 
• 83769-22-6 (1-Fluoro-cyclopentyl)-hydroxy-acetic acid ethyl ester 

Relevant academic research and scientific papers

HClO4·SiO2-mediated improved isomerization of glycidic esters to α-hydroxy-β,γ -unsaturated esters: Application in the formal synthesis of (R)-Baclofen and β-phenyl GABA analogues

An efficient isomerization of glycidic esters to corresponding allylic alcohols, viz. α-hydroxy-β,γ -unsaturated esters has been brought about using HClO4·SiO2. Five of these allylic alcohols underwent selective SN2' nucleophilic substitution to generate γ-azido-α,β-unsaturated esters which were readily converted to an antispastic drug Baclofen and four other β-phenyl GABA analogues.

A Total Synthesis of Allamcin. An Approach to Antileukaemic Iridoid Lactones and Formal Syntheses of Plumericin and Allamandin

A total synthesis of the iridoid lactone (+/-)-allamcin (3) found in Allamanda neriifolia is described.Starting from the readily available bicyclooctenone (10), the synthesis uses a strategy based on: (i) elaboration of the key acetoxy-aldhyde inte

Methode generale d'obtention des α-ceto esters β-fluores

A general method of synthesis of 3-alkyl (or aryl) 3-fluoro 2-oxo esters is described.The opening of glycidic esters with HF-pyridine (70percent w/w) followed by oxidation with Jones reagent, give the corresponding derivatives of fluoropyruvic esters in good yields.

NEW SYNTHETIC ROUTES TO β-FLUORO β-PHENYLLACTIC ACID DERIVATIVES AND Β-FLUOROCYANOHYDRINS

Alkyl phenyl 2,3-epoxycarboxylates from the well-known Darzens glycidic esters synthesis react under very mild conditions with pyridinium-poly-hydrogen fluoride to give corresponding 3-fluoro 3-phenyllactates in almost quantitative yields with a high regio and stereoselectivity.This method can be applied succesfully to other flycidic derivatives: glycidoamides, glycidonitriles, glycidoiminoesters...The spectrometric properties (IR, NMR) are presented.