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CAS 111821-49-9

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4-Borono-D-phenylalanine

Description:
4-Borono-D-phenylalanine (CAS 111821-49-9) is a non-natural amino acid that features a boronic acid group attached to the phenylalanine structure. This compound is characterized by its ability to form reversible covalent bonds with diols, making it particularly useful in biochemical applications, such as in the development of targeted drug delivery systems and in the study of protein interactions. The presence of the boron atom enhances its reactivity and specificity in various chemical reactions. 4-Borono-D-phenylalanine is often utilized in the synthesis of boron-containing compounds and in the field of medicinal chemistry, especially in the context of cancer research, where it can be used to target specific biomolecules. Additionally, its chirality (D-configuration) allows for unique interactions in biological systems, making it a valuable tool in the study of metabolic pathways and enzyme activity. Overall, this compound serves as an important building block in both synthetic and biological chemistry.
Formula:C9H12BNO4
InChI:InChI=1/C9H12BNO4/c11-8(9(12)13)5-6-1-3-7(4-2-6)10(14)15/h1-4,8,14-15H,5,11H2,(H,12,13)/t8-/m1/s1
SMILES:c1cc(ccc1C[C@H](C(=O)O)N)B(O)O
Synonyms:
  • 4-(dihydroxyboranyl)-D-phenylalanine
  • D-4-PHENYLALANINEBORONIC ACID
  • 4-BORONO-D-PHENYLALANINE
  • 4-BORONO-D-PHENYLALANINE 97%
  • 4-dihydroxyboryl-d-phenylalanine
  • (R)-2-AMino-3-(4-boronophenyl)propanoic acid
  • 4-Borono-D-phenylalanine B10
  • 4-BORONO-D-PHENYLALANINE B10 ENRICHED USP/EP/BP
  • 4-BORONO-D-PHENYLALANINE B10 ENRICHED
  • (2R)-2-amino-3-(4-boronophenyl)propanoic acid
  • See more synonyms
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