2-((tert-Butoxycarbonyl)amino)-5-(trifluoromethyl)benzoic acid
95%
- Product Code: 41186
CAS:
141940-29-6
| Molecular Weight: | 305.2498 g./mol | Molecular Formula: | C₁₃H₁₄F₃NO₄ |
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| EC Number: | MDL Number: | MFCD09859761 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a trifluoromethyl moiety, makes it valuable for constructing complex molecules. The Boc group can be selectively removed under mild acidic conditions, allowing for further functionalization of the molecule. The trifluoromethyl group enhances the lipophilicity and metabolic stability of the compounds it is incorporated into, which is beneficial in drug design. It is often employed in the synthesis of bioactive compounds, including potential therapeutic agents targeting various diseases. Additionally, its benzoic acid moiety provides a site for further chemical modifications, such as esterification or amidation, enabling the creation of diverse derivatives for research and development purposes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,834.00 |
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2-((tert-Butoxycarbonyl)amino)-5-(trifluoromethyl)benzoic acid
This chemical is primarily used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a trifluoromethyl moiety, makes it valuable for constructing complex molecules. The Boc group can be selectively removed under mild acidic conditions, allowing for further functionalization of the molecule. The trifluoromethyl group enhances the lipophilicity and metabolic stability of the compounds it is incorporated into, which is beneficial in drug design. It is often employed in the synthesis of bioactive compounds, including potential therapeutic agents targeting various diseases. Additionally, its benzoic acid moiety provides a site for further chemical modifications, such as esterification or amidation, enabling the creation of diverse derivatives for research and development purposes.
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