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759-67-1 | Ethyl 2-fluoro-3-oxopentanoate

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Ethyl 2-fluoro-3-oxopentanoate is a synthetic organic compound that has been used in various scientific and medical research applications. It is a colorless liquid with a molecular weight of 164.1 g/mol and a melting point of -51.7 °C. Ethyl 2-fluoro-3-oxopentanoate has a wide range of applications in the fields of che...

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CAS:759-67-1 | Ethyl 2-fluoro-3-oxopentanoate ,Description

Ethyl 2-fluoro-3-oxopentanoate is a synthetic organic compound that has been used in various scientific and medical research applications. It is a colorless liquid with a molecular weight of 164.1 g/mol and a melting point of -51.7 °C. Ethyl 2-fluoro-3-oxopentanoate has a wide range of applications in the fields of chemistry, biochemistry, and pharmacology.
 

Scientific Research Applications

 

C⋯π Interaction Studies

  • Research Insight: A study discovered an unusual C⋯π interaction of non-hydrogen bond type in ethyl (2Z)-2-cyano-3-[(3-fluoro-4-methoxyphenyl)amino]prop-2-enoate, contributing to the understanding of electrostatic interactions in such compounds (Zhang, Tong, Wu, & Zhang, 2012).

Synthesis of Pharmaceutical Intermediates

  • Research Insight: Ethyl 2-fluoro-3-oxopentanoate has been used as a raw material in the synthesis of 5-Fluoro-6-ethyl-4-hydroxy-pyrimidine, a key intermediate of voriconazole (Pan Xian-hua, 2013).

Agricultural Chemistry

  • Research Insight: The compound has been utilized in the synthesis of derivatives for use as gametocides in agricultural applications, particularly in inducing male sterility in plants (Iskra, Titan, & Meglič, 2013).

Combustion Kinetics and Biofuel Research

  • Research Insight: Ethyl levulinate, a derivative of Ethyl 2-fluoro-3-oxopentanoate, has been studied for its combustion kinetics, indicating potential as a biofuel component (Ghosh et al., 2018).

Enantioselective Synthesis

  • Research Insight: Studies have shown the use of Ethyl 2-fluoro-3-oxopentanoate in enantioselective synthesis, contributing to the development of chiral drugs and other compounds (Zhou, Ren, Zhang, Sun, & Wei, 2011).

Organic Synthesis and Chemical Reactions

  • Research Insight: Its derivatives have been applied in various organic synthesis reactions, including cycloaddition reactions and functionalization studies, which are fundamental in organic chemistry research (Patrick, Neumann, & Tatro, 2011).

Antimicrobial and Anticancer Research

  • Research Insight: Ethyl 2-fluoro-3-oxopentanoate derivatives have been explored for their potential in antimicrobial and anticancer applications, showing promise in medical research (Tiwari et al., 2018).

More Information

Product Name :Ethyl 2-fluoro-3-oxopentanoate
CAS No. :759-67-1Molecular Weight :162.16
MDL No. :MFCD09753153Purity/ Specification : 
Molecular Formula :C7H11FO3Storage :Sealed in dry,Store in freezer, under -20°C
Boiling Point :-  
GHS Pictogram : 
Signal Word :DangerPrecautionary Statements :P501-P260-P270-P264-P280-P303+P361+P353-P301+P330+P331-P363-P301+P312+P330-P304+P340+P310-P305+P351+P338+P310-P405
UN# :3265Class :8
Hazard Statements :H302-H314Packing Group :

 

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