2-(1-(tert-butoxycarbonyl)pyrrolidine-2-carboxamido)-[1,1'-biphenyl]-4,4'-dicarboxylic acid
98%
- Product Code: 41209
CAS:
1283676-82-3
| Molecular Weight: | 454.4724 g./mol | Molecular Formula: | C₂₄H₂₆N₂O₇ |
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| Density: | Storage Condition: | 2-8 ℃ airtight storage |
Product Description:
This compound is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceutical intermediates. Its structure, featuring a biphenyl dicarboxylic acid core and a tert-butoxycarbonyl-protected pyrrolidine moiety, makes it a valuable building block for constructing complex molecules. It is often employed in the synthesis of biologically active compounds, including potential drug candidates targeting various diseases. Additionally, its biphenyl group can be leveraged in the design of materials with specific electronic or optical properties, such as organic semiconductors or fluorescent probes. The tert-butoxycarbonyl (Boc) protecting group allows for selective deprotection, enabling precise control over chemical reactions during multi-step synthetic processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | £46.00 |
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| 0.500 | 10-20 days | £160.81 |
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| 1.000 | 10-20 days | £301.26 |
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2-(1-(tert-butoxycarbonyl)pyrrolidine-2-carboxamido)-[1,1'-biphenyl]-4,4'-dicarboxylic acid
This compound is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceutical intermediates. Its structure, featuring a biphenyl dicarboxylic acid core and a tert-butoxycarbonyl-protected pyrrolidine moiety, makes it a valuable building block for constructing complex molecules. It is often employed in the synthesis of biologically active compounds, including potential drug candidates targeting various diseases. Additionally, its biphenyl group can be leveraged in the design of materials with specific electronic or optical properties, such as organic semiconductors or fluorescent probes. The tert-butoxycarbonyl (Boc) protecting group allows for selective deprotection, enabling precise control over chemical reactions during multi-step synthetic processes.
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