CAS 1072945-97-1
:N-(3-Boronobenzoyl)glycine 1-ethyl ester
Description:
N-(3-Boronobenzoyl)glycine 1-ethyl ester is a chemical compound that features a boron-containing moiety, which is significant for its potential applications in medicinal chemistry and materials science. This compound is characterized by the presence of a boron atom bonded to a benzoyl group, which enhances its reactivity and ability to form complexes with various substrates. The glycine component contributes to its biological relevance, as glycine is an amino acid involved in numerous physiological processes. The ethyl ester functionality indicates that the compound can undergo hydrolysis to release glycine, making it potentially useful in drug delivery systems. Additionally, the presence of the boron atom may impart unique properties such as increased stability or enhanced interaction with biological targets. Overall, N-(3-Boronobenzoyl)glycine 1-ethyl ester is a versatile compound with implications in both synthetic and biological chemistry, particularly in the development of boron-based therapeutics and materials.
Formula:C11H14BNO5
InChI:InChI=1S/C11H14BNO5/c1-2-18-10(14)7-13-11(15)8-4-3-5-9(6-8)12(16)17/h3-6,16-17H,2,7H2,1H3,(H,13,15)
InChI key:InChIKey=WUHXILDYIOTKOQ-UHFFFAOYSA-N
SMILES:C(NCC(OCC)=O)(=O)C1=CC(B(O)O)=CC=C1
Synonyms:- [3-(2-Ethoxy-2-oxoethylcarbamoyl)phenyl]boronic acid
- N-(3-Boronobenzoyl)glycine 1-ethyl ester
- Glycine, N-(3-boronobenzoyl)-, 1-ethyl ester
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 2 products.
Ethyl (3-boronobenzoylamino)acetate
CAS:Ethyl (3-boronobenzoylamino)acetatePurity:≥95%Molecular weight:251.04g/mol

