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2-(Allyloxy)ethyl acetoacetate, with the molecular formula C11H16O4, is a versatile ester compound that features an acetoacetate group and an allyloxy group. It is recognized for its ability to form stable complexes with various metal ions, which makes it a valuable asset in coordination chemistry and catalysis. Moreover, its anti-inflammatory and antioxidant properties suggest potential medicinal applications, highlighting its significance in both industrial and research settings.

77757-00-7

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77757-00-7 Usage

Uses

Used in Pharmaceutical Synthesis:
2-(Allyloxy)ethyl acetoacetate is used as a key raw material for the synthesis of pharmaceuticals, leveraging its reactivity and complex-forming ability to create a variety of medicinal compounds.
Used in Agrochemical Production:
In the agrochemical industry, 2-(Allyloxy)ethyl acetoacetate serves as a crucial starting material, contributing to the development of effective crop protection agents and other agricultural products.
Used in Perfumery:
2-(Allyloxy)ethyl acetoacetate is utilized as a raw material in the creation of perfumes, capitalizing on its chemical structure to produce unique and desirable fragrances.
Used as a Solvent:
2-(Allyloxy)ethyl acetoacetate also functions as a solvent for a range of organic compounds, facilitating various chemical processes and reactions in different industries.
Used in Coordination Chemistry:
2-(Allyloxy)ethyl acetoacetate is employed as a ligand in coordination chemistry, forming stable complexes with metal ions, which is vital for the study and application of metal complexes in various chemical and material science domains.
Used in Catalysis:
Its application extends to catalysis, where it can act as a catalyst or a catalyst precursor, enhancing the efficiency of chemical reactions in industrial processes.
Potential Medicinal Applications:
Due to its anti-inflammatory and antioxidant properties, 2-(Allyloxy)ethyl acetoacetate is considered a potential candidate for medicinal applications, suggesting a future role in the development of new therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 77757-00-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,7,5 and 7 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 77757-00:
(7*7)+(6*7)+(5*7)+(4*5)+(3*7)+(2*0)+(1*0)=167
167 % 10 = 7
So 77757-00-7 is a valid CAS Registry Number.

77757-00-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Oxo-butyric acid 2-allyloxy-ethyl ester

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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More Details:77757-00-7 SDS

77757-00-7Downstream Products

77757-00-7Relevant academic research and scientific papers

Synthesis of bis-(3,5)pyrazolophanes by sequential intermolecular-intramolecular nitrilimine cycloadditions

Broggini, Gianluigi,Garanti, Luisa,Molteni, Giorgio,Zecchi, Gaetano

, p. 2843 - 2852 (2007/10/03)

A series of bis-(3,5)pyrazolophanes of potential interest in supramolecular chemistry have been synthesized by exploiting sequential intermolecular-intramolecular cycloadditions of properly functionalised nitrilimines.

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