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175278-22-5

Benzoic acid, 4-amino-3-(trifluoromethoxy)-

Catalog#: AR0021JN  |   CAS#: 175278-22-5  |   MDL#: MFCD00205143  |   MF: C8H6F3NO3  |   MW: 221.1333

Packsize Purity Price Availability Quantity
250mg 97% $5.00 Global Stock Buy Now Add To Cart
1g 97% $8.00 Global Stock Buy Now Add To Cart
5g 97% $23.00 Global Stock Buy Now Add To Cart
10g 97% $44.00 Global Stock Buy Now Add To Cart
25g 97% $106.00 Global Stock Buy Now Add To Cart
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Catalog Number AR0021JN
Chemical Name Benzoic acid, 4-amino-3-(trifluoromethoxy)-
CAS Number 175278-22-5
Molecular Formula C8H6F3NO3
Molecular Weight 221.1333
MDL Number MFCD00205143
SMILES Nc1ccc(cc1OC(F)(F)F)C(=O)O

The 4-Amino-3-(trifluoromethoxy)benzoic acid is a versatile building block in chemical synthesis due to its unique structure and reactivity. It serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and materials with various applications.1. Pharmaceutical Synthesis:
4-Amino-3-(trifluoromethoxy)benzoic acid is commonly used in the synthesis of pharmaceutical compounds due to its ability to introduce important functional groups into the target molecules. It can be further derivatized to create novel drug candidates with enhanced bioactivity and pharmacokinetic properties.2. Agrochemical Development:
In the field of agrochemicals, this compound plays a crucial role in the design and synthesis of crop protection agents. By incorporating the 4-amino and trifluoromethoxy moieties into the molecular structure, scientists can develop potent pesticides or herbicides that exhibit selective toxicity towards harmful pests while being environmentally friendly.3. Material Science:
4-Amino-3-(trifluoromethoxy)benzoic acid is also utilized in the preparation of advanced materials such as polymers, dyes, and functionalized surfaces. Its presence can modify the physical and chemical properties of the resulting materials, leading to improved performance characteristics in applications ranging from coatings to electronic devices.4. Chemical Research:
Researchers leverage the distinct reactivity of 4-Amino-3-(trifluoromethoxy)benzoic acid to conduct innovative chemical transformations in the laboratory. Its incorporation in synthetic routes allows for the creation of structurally diverse molecules that can be further explored for their potential biological or industrial activities.
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