401-55-8 | Ethyl Bromofluoroacetate

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$10.00	$7.00
5g	95%	in stock	$16.00	$11.00
10g	95%	in stock	$26.00	$18.00
25g	95%	in stock	$53.00	$37.00
100g	95%	in stock	$208.00	$145.00

Description

• Catalog Number: AB46101
• Chemical Name: Ethyl Bromofluoroacetate
• CAS Number: 401-55-8
• Molecular Formula: C4H6BrFO2
• Molecular Weight: 184.9916
• MDL Number: MFCD00042095
• SMILES: CCOC(=O)C(Br)F

Computed Properties

• Complexity: 86.1
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 8
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Undefined Atom Stereocenter Count: 1
• XLogP3: 1.3

Upstream Synthesis Route

Ethyl Bromofluoroacetate, also known as EBFA, is a valuable chemical compound widely utilized in various chemical synthesis processes. This versatile compound serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and specialty chemicals.In chemical synthesis, Ethyl Bromofluoroacetate is commonly employed as a reagent for introducing fluorine atoms into organic molecules. Its unique chemical properties make it particularly useful for the preparation of fluorinated compounds, which often exhibit enhanced biological activity and stability.Moreover, Ethyl Bromofluoroacetate can participate in a variety of reactions such as nucleophilic substitution, esterification, and Michael addition, expanding its utility in organic synthesis. Its compatibility with a range of functional groups and ability to selectively introduce fluorine atoms make it a valuable tool for the preparation of complex molecules with desired properties.Overall, Ethyl Bromofluoroacetate plays a crucial role in the synthesis of diverse chemical compounds, enabling researchers and chemists to efficiently access fluorinated derivatives for various applications in the fields of pharmaceuticals, agrochemicals, and materials science.

Literature

• Catalyzed Reformatsky reactions with ethyl bromofluoroacetate for the synthesis of alpha-fluoro-beta-hydroxy acids.

  The Journal of organic chemistry 20020111