Diethyl Fluoromalonate丨CAS 685-88-1

Diethyl Fluoromalonate丨CAS 685-88-1
Product Introduction:
Catalog No.: SS128741
CAS No.: 685-88-1
Purity (HNMR): 98.0%min
Product Name: Diethyl fluoromalonate
Molecular Formula: C7H11FO4
Molecular Weight: 178.16
Synonym(s): Diethyl 2-fluoromalonate; Fluoromalonic acid diethyl ester
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Technical Parameters
Description

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Specifications of Diethyl fluoromalonate丨CAS 685-88-1

 

Property

Specification

Purity (HNMR)

98.0%min

Appearance

Colorless or pale yellow transparent liquid

 

Transport Information of Diethyl fluoromalonate丨CAS 685-88-1

 

Parameter

Specification

UN Number

3265

Class

8

Packing Group

II

H.S. Code

2917190090304

Stability & Reactivity

The product is chemically stable under standard ambient conditions (room temperature).

Storage

Tightly closed. Store in a closed, dry, ventilated place

Condition to Avoid

 

Package

 

Diethyl fluoromalonate丨CAS 685-88-1 (DFM) is an organic fluorine compound with significant use in organic synthesis, particularly in the formation of fluorinated derivatives. It belongs to the class of malonates, which are esters of malonic acid. Diethyl fluoromalonate contains a fluorine atom attached to the central carbon of the malonate group, making it an important reagent in fluorination reactions. This chemical is used to introduce the fluorine atom into organic molecules, which can alter the molecular properties significantly.

 

Key Applications of Diethyl fluoromalonate丨CAS 685-88-1

 

1. Fluorination Reactions
● Fluorine Source: Diethyl fluoromalonate is primarily used as a fluorine source in organic reactions, specifically in the preparation of fluorinated organic compounds. Its reactive fluorine atom can be transferred to other organic molecules in nucleophilic substitution reactions.
● Pharmaceutical and Agrochemical Synthesis: It is used in the synthesis of fluorinated drugs and pesticides. Fluorination of organic compounds can enhance their metabolic stability, lipophilicity, and bioactivity. By replacing hydrogen with fluorine, compounds often gain increased potency, longer half-life, and better absorption.
2. Synthesis of Fluorinated Intermediates
● Intermediates in Chemical Synthesis: DFM serves as an important intermediate for the synthesis of more complex fluorinated compounds. It can react with a wide range of nucleophiles (such as amines and alcohols) to form fluorinated derivatives. These derivatives can then be further utilized in the synthesis of specialty chemicals.
● Building Block for Drug Development: The compound is often used to introduce fluorine atoms into drug-like molecules, particularly in medicinal chemistry, to improve their pharmacological properties.
3. Polymer Chemistry
● Fluorinated Polymers: Diethyl fluoromalonate丨CAS 685-88-1 is also utilized in the synthesis of fluorinated monomers, which can be polymerized to form fluoropolymers. Fluoropolymers are highly resistant to high temperatures, oxidation, and chemical degradation, making them ideal for specialized applications like coatings, insulating materials, and gaskets.
4. Synthesis of Fluorinated Malonates
● Malonate Derivatives: As a malonate ester, DFM is used in the synthesis of fluorinated malonates, which are important intermediates in the synthesis of fine chemicals and other specialized materials. These fluorinated malonates can undergo various reactions, such as alkylation and acylation, to form more complex structures.
5. Organic Synthesis and Research
● Reagent in Organic Chemistry: Diethyl fluoromalonate is used in academic and industrial research to explore new methods of fluorine incorporation into organic molecules. Its versatility as a fluorinating agent makes it an essential tool for chemists involved in the development of novel compounds with improved chemical stability and biological activity.

 

Benefits of Diethyl fluoromalonate丨CAS 685-88-1

 

1. Introduction of Fluorine Atom
● The key benefit of Diethyl fluoromalonate丨CAS 685-88-1 is its ability to introduce a fluorine atom into organic molecules. Fluorine substitution often leads to increased molecular stability, enhanced pharmacological activity, and improved physical properties (e.g., lipophilicity and biological half-life).
2. Improved Drug Properties
● The introduction of fluorine into pharmaceutical compounds often improves their binding affinity for biological targets, metabolic stability, and penetration of biological membranes. This is why DFM is widely used in drug development, especially for fluorinated drugs and radiopharmaceuticals.
3. Increased Potency in Agrochemicals
● In agrochemical synthesis, fluorination can increase the efficacy of pesticides and herbicides. Fluorine substitution can make these chemicals more potent, reduce environmental degradation, and improve selectivity for target organisms.
4. Versatility in Organic Synthesis
● DFM is a highly versatile reagent in organic synthesis. It can react with a wide range of nucleophiles and participate in various reactions such as alkylation, acylation, and condensation. This makes it an essential tool for synthesizing fluorinated intermediates and complex molecules.
5. Enhanced Stability of Fluoropolymers
● Fluoropolymers, made from fluorinated monomers like those derived from diethyl fluoromalonate, are thermally stable, resistant to chemical attack, and non-reactive in harsh environments. This gives rise to products used in applications where extreme conditions (such as high heat, chemical exposure, or mechanical wear) are a concern, such as insulation materials, coatings, and membranes.

 

Conclusion

 

Diethyl fluoromalonate丨CAS 685-88-1 is a highly valuable compound in organic synthesis due to its ability to introduce fluorine atoms into various organic molecules. Its primary applications lie in fluorination reactions, where it is used to synthesize fluorinated pharmaceuticals, agrochemicals, fluoropolymers, and specialty chemicals. The compound's ability to improve the stability, bioactivity, and potency of the molecules it modifies makes it an essential tool in the fields of medicinal chemistry, agrochemical development, and polymer science.

 

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