Ethyl 3-chloro-4-iodobenzoate

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Reagent Code: #45034
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CAS Number 874831-02-4

science Other reagents with same CAS 874831-02-4

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Weight 310.5161 g/mol
Formula C₉H₈ClIO₂
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MDL Number MFCD06637384
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Ethyl 3-chloro-4-iodobenzoate is primarily utilized in organic synthesis as a versatile intermediate for the preparation of more complex chemical compounds. Its structure, featuring both chloro and iodo substituents, makes it a valuable building block in the development of pharmaceuticals, agrochemicals, and specialty chemicals. The compound is often employed in cross-coupling reactions, such as Suzuki or Sonogashira couplings, to create biaryl or alkyne derivatives, which are essential in drug discovery and material science. Additionally, it serves as a precursor in the synthesis of active pharmaceutical ingredients (APIs) and fine chemicals, where its halogenated aromatic ring allows for further functionalization. Its use in research and industrial applications highlights its importance in advancing chemical innovation.

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inventory 100mg
10-20 days ฿1,278.00

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Ethyl 3-chloro-4-iodobenzoate
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Ethyl 3-chloro-4-iodobenzoate is primarily utilized in organic synthesis as a versatile intermediate for the preparation of more complex chemical compounds. Its structure, featuring both chloro and iodo substituents, makes it a valuable building block in the development of pharmaceuticals, agrochemicals, and specialty chemicals. The compound is often employed in cross-coupling reactions, such as Suzuki or Sonogashira couplings, to create biaryl or alkyne derivatives, which are essential in drug discovery

Ethyl 3-chloro-4-iodobenzoate is primarily utilized in organic synthesis as a versatile intermediate for the preparation of more complex chemical compounds. Its structure, featuring both chloro and iodo substituents, makes it a valuable building block in the development of pharmaceuticals, agrochemicals, and specialty chemicals. The compound is often employed in cross-coupling reactions, such as Suzuki or Sonogashira couplings, to create biaryl or alkyne derivatives, which are essential in drug discovery and material science. Additionally, it serves as a precursor in the synthesis of active pharmaceutical ingredients (APIs) and fine chemicals, where its halogenated aromatic ring allows for further functionalization. Its use in research and industrial applications highlights its importance in advancing chemical innovation.

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