430-99-9 | 2-Fluoroacrylic acid

Packsize	Purity	Availability	Price	Discounted Price
250mg	98%	in stock	$8.00	$5.00
1g	98%	in stock	$9.00	$7.00
5g	98%	in stock	$17.00	$12.00
10g	98%	in stock	$23.00	$17.00
25g	98%	in stock	$44.00	$31.00
100g	98%	in stock	$126.00	$89.00

Description

• Catalog Number: AB51578
• Chemical Name: 2-Fluoroacrylic acid
• CAS Number: 430-99-9
• Molecular Formula: C3H3FO2
• Molecular Weight: 90.0531
• MDL Number: MFCD03424474
• SMILES: FC(=C)C(=O)O

Computed Properties

• Complexity: 86.8
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 6
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 0.7

Upstream Synthesis Route

2-Fluoroacrylic acid, also known as alpha-fluoropropionic acid, is a versatile compound used in a variety of chemical synthesis applications. Its unique fluorine substitution offers distinct advantages in the production of pharmaceuticals, agrochemicals, and advanced materials.In chemical synthesis, 2-fluoroacrylic acid serves as a key building block for the creation of fluorinated organic compounds. Its fluorinated moiety imparts enhanced chemical and biological properties to the resulting molecules, making them valuable in drug discovery and development processes. By incorporating 2-fluoroacrylic acid into synthetic routes, chemists can modify the physicochemical properties of target molecules, such as enhancing bioavailability, metabolic stability, and binding affinity.Furthermore, 2-fluoroacrylic acid can be utilized in the synthesis of fluorinated polymers and materials with unique properties, including increased thermal stability, chemical resistance, and electrical conductivity. This compound's compatibility with various synthetic methodologies allows for the efficient construction of complex molecular structures, enabling researchers to design and fabricate innovative materials for diverse applications.Overall, 2-fluoroacrylic acid plays a crucial role in the field of chemical synthesis by facilitating the development of fluorinated compounds and advanced materials with enhanced properties and functionalities. Its versatility and utility make it a valuable asset for researchers and industries seeking to innovate and advance in various scientific disciplines.

Literature

• Asymmetric synthesis of enantiomerically and diastereoisomerically enriched 4-[F or Br]-substituted glutamic acids.

  Amino acids 20101101

• New matrix polymers for photo-activated resin composites using di-alpha-fluoroacrylic acid derivatives.

  Dental materials journal 20080701

• Diastereoselective Diels-Alder reactions of alpha-fluorinated alpha,beta-unsaturated carbonyl compounds: chemical consequences of fluorine substitution. 2.

  The Journal of organic chemistry 20020712