122455-36-1 | 2-Iodo-3-fluoronitrobenzene

Packsize	Purity	Availability	Price	Discounted Price
250mg	96%	in stock	$39.00	$27.00
1g	96%	in stock	$49.00	$34.00
5g	96%	in stock	$110.00	$77.00
25g	96%	in stock	$378.00	$264.00
100g	96%	in stock	$1,117.00	$782.00

Description

• Catalog Number: AA55871
• Chemical Name: 2-Iodo-3-fluoronitrobenzene
• CAS Number: 122455-36-1
• Molecular Formula: C6H3FINO2
• Molecular Weight: 266.9964
• MDL Number: MFCD07782082
• SMILES: [O-][N+](=O)c1cccc(c1I)F

Computed Properties

• Complexity: 161
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 3
• XLogP3: 2.5

Upstream Synthesis Route

1-Fluoro-2-iodo-3-nitrobenzene is a versatile compound commonly used in chemical synthesis for its unique properties and reactivity. As a key building block in organic synthesis, this compound serves as a valuable precursor in the preparation of various complex organic molecules. Its strategic placement of functional groups makes it particularly useful in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals.One of the primary applications of 1-Fluoro-2-iodo-3-nitrobenzene is in the field of medicinal chemistry, where it can be employed to introduce specific structural motifs into drug candidates. By undergoing various chemical transformations, this compound can be modified to generate novel derivatives with potential biological activity. Its nitro and halogen functionalities enable it to participate in a range of substitution, elimination, and coupling reactions, allowing chemists to access diverse chemical space for drug discovery.Furthermore, 1-Fluoro-2-iodo-3-nitrobenzene plays a crucial role in material science for the synthesis of advanced materials such as liquid crystals, dyes, and polymers. Its ability to undergo selective transformations under controlled conditions enables the design and fabrication of functional materials with tailored properties. By incorporating this compound into polymerization processes or functionalizing its aromatic ring, researchers can develop innovative materials for various applications in electronics, optoelectronics, and photonics.Overall, the versatile nature of 1-Fluoro-2-iodo-3-nitrobenzene makes it an indispensable tool in organic synthesis, offering chemists a versatile building block for the creation of complex molecules with diverse functionalities and applications.