2,2-difluoro-2-(3-hydroxyphenyl)acetic acid
96%
- Product Code: 74558
CAS:
1785497-82-6
Molecular Weight: | 188.13 g./mol | Molecular Formula: | C₈H₆F₂O₃ |
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EC Number: | MDL Number: | ||
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8℃ |
Product Description:
Primarily utilized in the pharmaceutical industry, this compound serves as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its unique structure, featuring both difluoro and hydroxyphenyl groups, makes it valuable in the development of drugs targeting specific enzymes or receptors.
In medicinal chemistry, it is often employed in the creation of anti-inflammatory and analgesic agents, where the hydroxyphenyl moiety can interact with biological targets to modulate their activity. Additionally, the difluoro substitution enhances the metabolic stability and bioavailability of the resulting drug molecules, making it a preferred choice in drug design.
Beyond pharmaceuticals, this chemical finds application in agrochemical research, where it is used to develop novel herbicides and pesticides. The difluoroacetic acid group contributes to the efficacy of these compounds by improving their binding affinity to target proteins in pests or weeds.
Its role in organic synthesis is also noteworthy, as it can act as a building block for more complex molecules, particularly in the construction of fluorinated aromatic compounds, which are increasingly important in materials science and specialty chemicals.
Product Specification:
Test | Specification |
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APPEARANCE | Yellow solid |
PURITY | 95.5-100 |
Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | ฿5,050.00 |
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1.000 | 10-20 days | ฿14,410.00 |
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2,2-difluoro-2-(3-hydroxyphenyl)acetic acid
Primarily utilized in the pharmaceutical industry, this compound serves as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its unique structure, featuring both difluoro and hydroxyphenyl groups, makes it valuable in the development of drugs targeting specific enzymes or receptors.
In medicinal chemistry, it is often employed in the creation of anti-inflammatory and analgesic agents, where the hydroxyphenyl moiety can interact with biological targets to modulate their activity. Additionally, the difluoro substitution enhances the metabolic stability and bioavailability of the resulting drug molecules, making it a preferred choice in drug design.
Beyond pharmaceuticals, this chemical finds application in agrochemical research, where it is used to develop novel herbicides and pesticides. The difluoroacetic acid group contributes to the efficacy of these compounds by improving their binding affinity to target proteins in pests or weeds.
Its role in organic synthesis is also noteworthy, as it can act as a building block for more complex molecules, particularly in the construction of fluorinated aromatic compounds, which are increasingly important in materials science and specialty chemicals.
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