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666746-27-6

N-Boc-4-iodo-2-methylaniline

Catalog#: AR003TIG  |   CAS#: 666746-27-6  |   MDL#: MFCD08703145  |   MF: C12H16INO2  |   MW: 333.1654

Packsize Purity Price Availability Quantity
100mg 97% $15.00 Global Stock Buy Now Add To Cart
250mg 97% $16.00 Global Stock Buy Now Add To Cart
1g 97% $43.00 Global Stock Buy Now Add To Cart
5g 97% $176.00 Global Stock Buy Now Add To Cart
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Catalog Number AR003TIG
Chemical Name N-Boc-4-iodo-2-methylaniline
CAS Number 666746-27-6
Molecular Formula C12H16INO2
Molecular Weight 333.1654
MDL Number MFCD08703145
SMILES O=C(OC(C)(C)C)Nc1ccc(cc1C)I

N-Boc-4-iodo-2-methylaniline, also known as Boc-protected 4-iodo-2-methylaniline, is a versatile compound commonly used in organic synthesis. With a tert-butoxycarbonyl (Boc) protective group on the amine nitrogen and an iodine atom at the 4-position of the aromatic ring, this compound offers unique reactivity and selectivity in various chemical reactions.In chemical synthesis, N-Boc-4-iodo-2-methylaniline serves as a valuable building block for the creation of complex molecules. The Boc protecting group blocks the reactivity of the amine, allowing selective manipulation of other functional groups within a molecule. This strategic protection-deprotection approach is particularly useful in multistep synthesis, where the timing and order of reactions are crucial.The presence of the iodine atom in N-Boc-4-iodo-2-methylaniline also confers specific reactivity benefits. Iodine is a versatile halogen atom that can participate in various transformations, such as nucleophilic substitution and transition metal-catalyzed reactions. The 4-iodo substitution pattern further influences the electronic properties of the aromatic ring, leading to tailored reactivity in coupling reactions or aromatic substitutions.Overall, N-Boc-4-iodo-2-methylaniline is a valuable tool in the toolbox of organic chemists for the synthesis of target molecules with precise control over regioselectivity, stereochemistry, and functional group compatibility. Its strategic incorporation can streamline complex synthesis routes and enable the efficient construction of diverse molecular architectures.
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GHS Pictogram
Signal Word Warning
UN# N/A
Hazard Statements H302
Precautionary Statements P264-P270-P301+P312-P330
Class N/A
Packing Group N/A

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