1197193-11-5 | 2-Fluoro-4-(methylsulfonyl)benzaldehyde

Packsize	Purity	Availability	Price	Discounted Price
250mg	95%	in stock	$114.00	$80.00
1g	95%	in stock	$123.00	$86.00
5g	95%	in stock	$380.00	$266.00
10g	95%	in stock	$713.00	$499.00
25g	95%	in stock	$1,490.00	$1,043.00

Description

• Catalog Number: AA32887
• Chemical Name: 2-Fluoro-4-(methylsulfonyl)benzaldehyde
• CAS Number: 1197193-11-5
• Molecular Formula: C8H7FO3S
• Molecular Weight: 202.2028
• MDL Number: MFCD13191594
• SMILES: O=Cc1ccc(cc1F)S(=O)(=O)C

Computed Properties

• Complexity: 280
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 2
• XLogP3: 0.7

Upstream Synthesis Route

2-Fluoro-4-(methylsulfonyl)benzaldehyde is a key intermediate widely used in organic synthesis due to its versatile reactivity and unique properties. In chemical synthesis, this compound serves as a valuable building block for the construction of various complex molecules and pharmaceutical compounds. One notable application of 2-Fluoro-4-(methylsulfonyl)benzaldehyde is in the synthesis of heterocyclic compounds such as benzimidazoles and benzothiazoles. The aldehyde group allows for easy functionalization through various reactions, enabling the introduction of different substituents and functionalities to tailor the properties of the final compound. Additionally, the presence of the fluoro and methylsulfonyl groups imparts specific characteristics to the molecule, making it a desirable precursor in the development of novel materials and bioactive compounds.Furthermore, the electron-withdrawing nature of the fluoro and sulfonyl groups in 2-Fluoro-4-(methylsulfonyl)benzaldehyde makes it a valuable reagent in aromatic substitution reactions. These groups enhance the electrophilic character of the benzene ring, promoting regioselective reactions and facilitating the formation of diverse derivatives with high efficiency.Overall, the strategic placement of functional groups in 2-Fluoro-4-(methylsulfonyl)benzaldehyde empowers synthetic chemists with the tools to access a wide array of chemical transformations, making it an indispensable component in the toolkit of organic chemists and researchers.