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CAS 243448-17-1

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α-Amino-2,5-difluorobenzeneacetic acid

Description:
α-Amino-2,5-difluorobenzeneacetic acid, with the CAS number 243448-17-1, is an organic compound characterized by the presence of an amino group and a carboxylic acid functional group attached to a benzene ring that has two fluorine substituents at the 2 and 5 positions. This compound typically exhibits properties associated with both amino acids and aromatic compounds, such as solubility in polar solvents and potential for hydrogen bonding due to the amino and carboxylic acid groups. The fluorine atoms can influence the compound's reactivity, stability, and biological activity, often enhancing lipophilicity and altering electronic properties. Its structure suggests potential applications in pharmaceuticals, particularly in the development of drugs that target specific biological pathways. Additionally, the presence of fluorine can improve metabolic stability and bioavailability. Overall, α-Amino-2,5-difluorobenzeneacetic acid represents a unique class of compounds with diverse chemical and biological implications.
Formula:C8H7F2NO2
InChI:InChI=1S/C8H7F2NO2/c9-4-1-2-6(10)5(3-4)7(11)8(12)13/h1-3,7H,11H2,(H,12,13)
InChI key:InChIKey=FSTDRNWTSCJIRN-UHFFFAOYSA-N
SMILES:C(C(O)=O)(N)C1=C(F)C=CC(F)=C1
Synonyms:
  • 2,5-Difluoro-<span class="text-smallcaps">D</smallcap><smallcap>L</span>-phenyLglycine
  • 2-Amino-2-(2,5-difluorophenyl)acetic acid
  • 3-(Thiophen-2-Yl)Isoxazol-5-Amine
  • 3-Thiophen-2-Yl-Isoxazol-5-Ylamine
  • Salor-Int L482994-1Ea
  • α-Amino-2,5-difluorobenzeneacetic acid
  • Benzeneacetic acid, α-amino-2,5-difluoro-
  • 2,5-Difluoro-DL-phenyLglycine
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