101335-11-9 | 2-Chloro-4-fluoroiodobenzene

Packsize	Purity	Availability	Price	Discounted Price
5g	97%	in stock	$7.00	$5.00
10g	97%	in stock	$12.00	$9.00
100g	97%	in stock	$82.00	$57.00
500g	97%	in stock	$329.00	$230.00

Description

• Catalog Number: AA05322
• Chemical Name: 2-Chloro-4-fluoroiodobenzene
• CAS Number: 101335-11-9
• Molecular Formula: C6H3ClFI
• Molecular Weight: 256.4439
• MDL Number: MFCD00051774
• SMILES: Fc1ccc(c(c1)Cl)I

Computed Properties

• Complexity: 99.1
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 9
• Hydrogen Bond Acceptor Count: 1
• XLogP3: 3.3

Upstream Synthesis Route

2-Chloro-4-fluoro-1-iodobenzene, also known as $name$, is a valuable chemical compound widely used in various applications in chemical synthesis. This versatile compound serves as a key building block in the production of pharmaceuticals, agrochemicals, and materials science. Its strategic positioning of halogen substituents makes it a crucial intermediate in the synthesis of complex organic molecules.In chemical synthesis, 2-Chloro-4-fluoro-1-iodobenzene plays a vital role as a reactive intermediate due to its unique reactivity pattern. The presence of multiple halogen atoms confers a high degree of electrophilicity, allowing for facile substitution reactions with a variety of nucleophiles. This reactivity makes it an ideal precursor for introducing functional groups such as amines, alcohols, and thiols into target molecules.Furthermore, the specific arrangement of halogens in 2-Chloro-4-fluoro-1-iodobenzene imparts regioselectivity in sequential reactions, enabling the controlled synthesis of complex molecular structures. Its compatibility with various coupling methodologies, such as Suzuki-Miyaura, Negishi, and Stille couplings, makes it a preferred choice in the construction of carbon-carbon and carbon-heteroatom bonds.Overall, the application of 2-Chloro-4-fluoro-1-iodobenzene in chemical synthesis is instrumental in the efficient design and preparation of advanced organic compounds with diverse functionalities. Its versatility and reactivity make it a valuable tool for synthetic chemists seeking to create novel molecules for pharmaceutical, agricultural, and material science applications.