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CAS 913835-72-0

:

3-Borono-5-[[(1,1-dimethylethoxy)carbonyl]amino]benzoic acid

Description:
3-Borono-5-[[(1,1-dimethylethoxy)carbonyl]amino]benzoic acid is a chemical compound characterized by its boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, particularly in medicinal chemistry and organic synthesis. The presence of the 1,1-dimethylethoxycarbonyl group indicates that the compound has a protective group that can be removed under specific conditions, allowing for further functionalization of the molecule. This compound features a benzoic acid moiety, which contributes to its acidity and potential reactivity. Its structure suggests that it may be involved in biological processes or serve as a building block in the synthesis of more complex molecules. Additionally, the boron atom can enhance the compound's properties in terms of reactivity and selectivity in chemical reactions. Overall, 3-Borono-5-[[(1,1-dimethylethoxy)carbonyl]amino]benzoic acid is a versatile compound with significant implications in both research and industrial applications.
Formula:C12H16BNO6
InChI:InChI=1/C12H16BNO6/c1-12(2,3)20-11(17)14-9-5-7(10(15)16)4-8(6-9)13(18)19/h4-6,18-19H,1-3H3,(H,14,17)(H,15,16)
InChI key:InChIKey=DDZVPNHBJRCXEI-UHFFFAOYSA-N
SMILES:N(C(OC(C)(C)C)=O)C1=CC(B(O)O)=CC(C(O)=O)=C1
Synonyms:
  • 3-[[(tert-Butoxy)carbonyl]amino]-5-(dihydroxyboranyl)benzoic acid
  • 3-Borono-5-((tert-butoxycarbonyl)amino)benzoic acid
  • 3-Borono-5-[[(1,1-dimethylethoxy)carbonyl]amino]benzoic acid
  • 3-Borono-5-((tert-butoxycarbonyl)amino)benzoicacid
  • Benzoic acid, 3-borono-5-[[(1,1-dimethylethoxy)carbonyl]amino]-
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