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6277-17-4

2-Iodo-1-methyl-3-nitrobenzene

Catalog#: AR003I5E  |   CAS#: 6277-17-4  |   MDL#: MFCD00091040  |   MF: C7H6INO2  |   MW: 263.0325

Packsize Purity Price Availability Quantity
1g 98% $5.00 Global Stock Buy Now Add To Cart
5g 98% $16.00 Global Stock Buy Now Add To Cart
25g 98% $77.00 Global Stock Buy Now Add To Cart
100g 98% $293.00 Global Stock Buy Now Add To Cart
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Catalog Number AR003I5E
Chemical Name 2-Iodo-1-methyl-3-nitrobenzene
CAS Number 6277-17-4
Molecular Formula C7H6INO2
Molecular Weight 263.0325
MDL Number MFCD00091040
SMILES [O-][N+](=O)c1cccc(c1I)C
NSC Number 35343

2-Iodo-1-methyl-3-nitrobenzene is a versatile compound used in chemical synthesis due to its unique properties and reactivity. This compound is commonly employed as a key building block in the synthesis of various pharmaceuticals, agrochemicals, and advanced materials. Its iodo and nitro substituents make it an excellent candidate for further functionalization through various chemical reactions, allowing for the development of diverse molecular structures.In organic synthesis, 2-Iodo-1-methyl-3-nitrobenzene can serve as a precursor for the introduction of functional groups such as amines, aldehydes, ketones, and carboxylic acids. Additionally, its iodo group can undergo cross-coupling reactions with different organic substrates, enabling the formation of complex molecules with tailored properties. The nitro group can also undergo reduction reactions to yield amino derivatives, expanding the compound's potential applications in medicinal chemistry and materials science.Furthermore, the presence of the methyl group provides steric hindrance that can influence the regioselectivity and stereoselectivity of subsequent reactions, making this compound a valuable tool for controlling the outcome of chemical transformations. Overall, 2-Iodo-1-methyl-3-nitrobenzene plays a crucial role in the synthesis of diverse organic compounds and offers synthetic chemists a wide range of possibilities for designing and accessing new molecules with desired functionalities.
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