2-(Boc-amino)-2-(4-bromophenyl)acetic Acid
≥97%
- Product Code: 58265
CAS:
917925-71-4
| Molecular Weight: | 330.17 g./mol | Molecular Formula: | C₁₃H₁₆BrNO₄ |
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| EC Number: | MDL Number: | MFCD04115515 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily used in organic synthesis, particularly in the pharmaceutical and biotechnology industries. It serves as a key intermediate in the production of various biologically active molecules. Its Boc (tert-butoxycarbonyl) protecting group allows for selective deprotection, enabling the synthesis of complex peptides and small molecules. The presence of the 4-bromophenyl group makes it valuable in cross-coupling reactions, such as Suzuki or Heck reactions, which are essential for constructing carbon-carbon bonds in drug development. It is also utilized in the preparation of chiral compounds, aiding in the study of enantioselective reactions and the development of asymmetric catalysts.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.250 | 10-20 days | $327.57 |
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| 1.000 | 10-20 days | $736.30 |
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2-(Boc-amino)-2-(4-bromophenyl)acetic Acid
This compound is primarily used in organic synthesis, particularly in the pharmaceutical and biotechnology industries. It serves as a key intermediate in the production of various biologically active molecules. Its Boc (tert-butoxycarbonyl) protecting group allows for selective deprotection, enabling the synthesis of complex peptides and small molecules. The presence of the 4-bromophenyl group makes it valuable in cross-coupling reactions, such as Suzuki or Heck reactions, which are essential for constructing carbon-carbon bonds in drug development. It is also utilized in the preparation of chiral compounds, aiding in the study of enantioselective reactions and the development of asymmetric catalysts.
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