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

95%

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

science Other reagents with same CAS 1540188-38-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 249.4890 g/mol
Formula C₈H₆BrClO₂
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MDL Number MFCD24108594
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description Product Description

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.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿4,023.00
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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