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69705-29-9

4-Chloro-2-iodo-6-methylaniline

Catalog#: AR005JKN  |   CAS#: 69705-29-9  |   MDL#: MFCD16622764  |   MF: C7H7ClIN  |   MW: 267.4947

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Catalog Number AR005JKN
Chemical Name 4-Chloro-2-iodo-6-methylaniline
CAS Number 69705-29-9
Molecular Formula C7H7ClIN
Molecular Weight 267.4947
MDL Number MFCD16622764
SMILES Clc1cc(C)c(c(c1)I)N

4-Chloro-2-iodo-6-methylaniline is a versatile compound commonly used in chemical synthesis as a key building block in the production of various pharmaceuticals, agrochemicals, and dyes. Due to its unique structure and reactivity, this compound serves as a valuable intermediate in the synthesis of complex organic molecules.In organic chemistry, 4-Chloro-2-iodo-6-methylaniline can be utilized in the preparation of heterocyclic compounds, which are important structural motifs found in a wide range of bioactive molecules. Its halogen substituents enable selective functionalization reactions, allowing for the introduction of diverse chemical groups to tailor the properties of the final product.Moreover, this compound can participate in various cross-coupling reactions, such as Suzuki-Miyaura coupling or Buchwald-Hartwig amination, to form carbon-carbon or carbon-nitrogen bonds. These transformations are crucial for creating new carbon-carbon frameworks and incorporating nitrogen-containing functionalities in organic molecules.Additionally, 4-Chloro-2-iodo-6-methylaniline can serve as a precursor for the synthesis of dyes and pigments, where its aromatic structure contributes to the color properties of the final product. By manipulating the substituents on the aromatic ring, chemists can modulate the hue and intensity of the resulting dye, making this compound valuable in the colorant industry.Overall, the application of 4-Chloro-2-iodo-6-methylaniline in chemical synthesis showcases its significance as a versatile building block for constructing complex organic molecules with diverse functionalities and applications.
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GHS Pictogram N/A
UN# -
Hazard Statements -
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