7292-73-1 | 4-Fluoro-DL-phenylglycine

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$16.00	$11.00
10g	97%	in stock	$33.00	$23.00
25g	97%	in stock	$81.00	$57.00
100g	97%	in stock	$249.00	$175.00

Description

• Catalog Number: AB67566
• Chemical Name: 4-Fluoro-DL-phenylglycine
• CAS Number: 7292-73-1
• Molecular Formula: C8H8FNO2
• Molecular Weight: 169.153
• MDL Number: MFCD00066444
• SMILES: NC(c1ccc(cc1)F)C(=O)O
• NSC Number: 101466

Computed Properties

• Complexity: 166
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 2
• Undefined Atom Stereocenter Count: 1
• XLogP3: -1.6

Upstream Synthesis Route

4-Fluorophenylglycine, also known as Fpg, is a valuable building block in chemical synthesis due to its versatile reactivity and unique structural properties. This compound is commonly used as a precursor in the synthesis of various pharmaceuticals, agrochemicals, and materials.In chemical synthesis, 4-Fluorophenylglycine serves as a key intermediate in the preparation of diverse compounds with fluorine substitution, which imparts specific physical and chemical properties to the final products. Its incorporation into molecule structures can enhance their biological activity, stability, and solubility, making it a crucial component in medicinal chemistry and drug development.Moreover, 4-Fluorophenylglycine can be utilized in the synthesis of chiral compounds, as its stereochemistry can be manipulated to control the enantiomeric purity of the final products. This makes it a valuable tool in asymmetric synthesis and the production of enantiomerically pure compounds for pharmaceutical applications.Overall, 4-Fluorophenylglycine plays a vital role in chemical synthesis by enabling the efficient and tailored construction of complex molecules with enhanced properties for various industrial and research purposes.

Literature

• 4-fluorophenylglycine as a label for 19F NMR structure analysis of membrane-associated peptides.

  Chembiochem : a European journal of chemical biology 20031107