2-(3-Bromo-4-chlorophenyl)acetic acid
97%
- Product Code: 45230
CAS:
90004-80-1
| Molecular Weight: | 249.49 g./mol | Molecular Formula: | C₈H₆BrClO₂ |
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| EC Number: | MDL Number: | MFCD18390582 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
This compound is primarily utilized in organic synthesis as an intermediate for the production of various pharmaceuticals and agrochemicals. Its structure, featuring both bromo and chloro substituents on the phenyl ring, makes it a versatile building block for constructing more complex molecules. It is often employed in the development of active pharmaceutical ingredients (APIs) where specific halogenated aromatic systems are required. Additionally, it can be used in research settings to study the effects of halogenation on the biological activity of organic compounds. Its application extends to the synthesis of herbicides and other crop protection agents, leveraging its reactivity in coupling reactions and functional group transformations.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.250 | 10-20 days | $29.38 |
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| 1.000 | 10-20 days | $73.23 |
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| 5.000 | 10-20 days | $217.88 |
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| 10.000 | 10-20 days | $362.08 |
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2-(3-Bromo-4-chlorophenyl)acetic acid
This compound is primarily utilized in organic synthesis as an intermediate for the production of various pharmaceuticals and agrochemicals. Its structure, featuring both bromo and chloro substituents on the phenyl ring, makes it a versatile building block for constructing more complex molecules. It is often employed in the development of active pharmaceutical ingredients (APIs) where specific halogenated aromatic systems are required. Additionally, it can be used in research settings to study the effects of halogenation on the biological activity of organic compounds. Its application extends to the synthesis of herbicides and other crop protection agents, leveraging its reactivity in coupling reactions and functional group transformations.
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