4-Chloro-5-iodo-2-methoxybenzoic acid

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Reagent Code: #47171
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CAS Number 1440526-64-6

science Other reagents with same CAS 1440526-64-6

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Weight 312.4800 g/mol
Formula C₈H₆O₃ClI
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MDL Number MFCD24843099
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4-Chloro-5-iodo-2-methoxybenzoic acid is primarily utilized in organic synthesis as a versatile intermediate for the preparation of more complex chemical compounds. Its unique structure, featuring both chloro and iodo substituents, makes it valuable in cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential in pharmaceutical and agrochemical research. The methoxy group further enhances its reactivity, allowing for selective functionalization in the synthesis of bioactive molecules. Additionally, it serves as a building block in the development of dyes, pigments, and materials with specific optical properties. Its applications are particularly prominent in medicinal chemistry, where it contributes to the creation of potential drug candidates targeting various diseases.

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inventory 100mg
10-20 days ฿1,395.00

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4-Chloro-5-iodo-2-methoxybenzoic acid
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4-Chloro-5-iodo-2-methoxybenzoic acid is primarily utilized in organic synthesis as a versatile intermediate for the preparation of more complex chemical compounds. Its unique structure, featuring both chloro and iodo substituents, makes it valuable in cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential in pharmaceutical and agrochemical research. The methoxy group further enhances its reactivity, allowing for selective functionalization in the synthesis of bioactive mo

4-Chloro-5-iodo-2-methoxybenzoic acid is primarily utilized in organic synthesis as a versatile intermediate for the preparation of more complex chemical compounds. Its unique structure, featuring both chloro and iodo substituents, makes it valuable in cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential in pharmaceutical and agrochemical research. The methoxy group further enhances its reactivity, allowing for selective functionalization in the synthesis of bioactive molecules. Additionally, it serves as a building block in the development of dyes, pigments, and materials with specific optical properties. Its applications are particularly prominent in medicinal chemistry, where it contributes to the creation of potential drug candidates targeting various diseases.

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