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683238-59-7

2-Chloro-1-iodo-3-nitrobenzene

Catalog#: AR01X01S  |   CAS#: 683238-59-7  |   MDL#: MFCD15527334  |   MF: C6H3ClINO2  |   MW: 283.451

Packsize Purity Price Availability Quantity
100mg 98% $125.00 Global Stock Buy Now Add To Cart
250mg 98% $208.00 Global Stock Buy Now Add To Cart
1g 98% $416.00 Global Stock Buy Now Add To Cart
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Catalog Number AR01X01S
Chemical Name 2-Chloro-1-iodo-3-nitrobenzene
CAS Number 683238-59-7
Molecular Formula C6H3ClINO2
Molecular Weight 283.451
MDL Number MFCD15527334
SMILES [O-][N+](=O)c1cccc(c1Cl)I

2-Chloro-1-iodo-3-nitrobenzene is a versatile compound widely used in chemical synthesis for its unique properties and reactivity. This compound serves as a valuable building block in the synthesis of various organic compounds due to the presence of both chlorine and iodine atoms, as well as the nitro group, which provide opportunities for a range of functional group transformations.In organic synthesis, 2-Chloro-1-iodo-3-nitrobenzene can be utilized as a key intermediate in the preparation of pharmaceuticals, agrochemicals, and fine chemicals. Its ability to undergo nucleophilic aromatic substitution reactions enables the introduction of different functional groups at the ortho, meta, or para positions of the benzene ring, allowing for the creation of complex molecular structures.Furthermore, the presence of the nitro group in the molecule offers potential for further transformations, such as reduction to an amino group or conversion to other functionalities, expanding the versatility of this compound in synthetic routes. Additionally, the dual halogenation pattern of chlorine and iodine in 2-Chloro-1-iodo-3-nitrobenzene enables selective cross-coupling reactions with various organometallic reagents in transition metal-catalyzed reactions, facilitating the formation of carbon-carbon and carbon-heteroatom bonds.Overall, the strategic incorporation of 2-Chloro-1-iodo-3-nitrobenzene in chemical synthesis allows for the synthesis of diverse organic molecules with tailored structures and properties, making it a valuable tool for organic chemists in designing efficient synthetic pathways.
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