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CAS 73086-97-2

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Benzenepropanoic acid, α-(aminooxy)-, hydrobromide, (S)-

Description:
Benzenepropanoic acid, α-(aminooxy)-, hydrobromide, (S)-, is a chemical compound characterized by its aminooxy functional group, which is known for its ability to form stable covalent bonds with carbonyl compounds, making it useful in various biochemical applications. The presence of the benzene ring contributes to its hydrophobic characteristics, while the propanoic acid moiety provides acidic properties. The hydrobromide salt form indicates that the compound is protonated, enhancing its solubility in polar solvents, which is advantageous for biological and chemical reactions. The (S)- designation refers to its specific stereochemistry, indicating that it is the S-enantiomer, which can have distinct biological activity compared to its R counterpart. This compound may be utilized in research related to drug development, particularly in the synthesis of compounds that interact with biological targets through covalent modification. Its unique structure and properties make it a valuable tool in medicinal chemistry and biochemistry.
Formula:C9H11NO3·BrH
InChI:InChI=1S/C9H11NO3.BrH/c10-13-8(9(11)12)6-7-4-2-1-3-5-7;/h1-5,8H,6,10H2,(H,11,12);1H/t8-;/m0./s1
InChI key:InChIKey=YENJJZAVLSPBIZ-QRPNPIFTSA-N
SMILES:C([C@@H](C(O)=O)ON)C1=CC=CC=C1.Br
Synonyms:
  • (2S)-2-(Aminooxy)-3-phenylpropanoic acid hydrobromide
  • Benzenepropanoic acid, α-(aminooxy)-, hydrobromide, (S)-
  • Carboxy(3-Phenylpropoxy)Ammonium Bromide
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