5-Bromo-3-chloro-2-methylbenzoic acid

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Reagent Code: #48978
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CAS Number 1540188-38-2

science Other reagents with same CAS 1540188-38-2

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Weight 249.4890 g/mol
Formula C₈H₆BrClO₂
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MDL Number MFCD24108594
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5-Bromo-3-chloro-2-methylbenzoic acid finds application in organic synthesis as a versatile intermediate. It is commonly used in the development of pharmaceuticals and agrochemicals due to its unique substitution pattern, which allows for further functionalization. The compound serves as a building block in the synthesis of more complex molecules, particularly in the creation of active pharmaceutical ingredients (APIs) and herbicides. Its halogenated structure makes it valuable in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, which are essential in medicinal chemistry. Additionally, it can be utilized in the preparation of dyes, pigments, and other specialty chemicals where specific aromatic frameworks are required.

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inventory 100mg
10-20 days ฿4,023.00

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5-Bromo-3-chloro-2-methylbenzoic acid
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5-Bromo-3-chloro-2-methylbenzoic acid finds application in organic synthesis as a versatile intermediate. It is commonly used in the development of pharmaceuticals and agrochemicals due to its unique substitution pattern, which allows for further functionalization. The compound serves as a building block in the synthesis of more complex molecules, particularly in the creation of active pharmaceutical ingredients (APIs) and herbicides. Its halogenated structure makes it valuable in cross-coupling reaction

5-Bromo-3-chloro-2-methylbenzoic acid finds application in organic synthesis as a versatile intermediate. It is commonly used in the development of pharmaceuticals and agrochemicals due to its unique substitution pattern, which allows for further functionalization. The compound serves as a building block in the synthesis of more complex molecules, particularly in the creation of active pharmaceutical ingredients (APIs) and herbicides. Its halogenated structure makes it valuable in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, which are essential in medicinal chemistry. Additionally, it can be utilized in the preparation of dyes, pigments, and other specialty chemicals where specific aromatic frameworks are required.

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