CymitQuimica logo

CAS 175203-83-5

:

N-(2-Furanylmethyl)-β-alanine ethyl ester

Description:
N-(2-Furanylmethyl)-β-alanine ethyl ester is an organic compound characterized by its unique structure, which includes a furan ring and an ethyl ester functional group. This compound features a β-alanine backbone, which is an amino acid known for its role in various biological processes. The presence of the furan moiety contributes to its potential reactivity and biological activity, making it of interest in medicinal chemistry and organic synthesis. Typically, compounds like this may exhibit properties such as solubility in organic solvents, moderate stability under standard conditions, and potential interactions with biological targets due to the presence of both the amino and ester functional groups. Its applications could range from pharmaceuticals to agrochemicals, depending on its specific reactivity and biological activity. As with many organic compounds, safety and handling precautions should be observed, particularly regarding its potential toxicity and reactivity. Further studies would be necessary to fully elucidate its properties and potential applications in various fields.
Formula:C10H15NO3
InChI:InChI=1/C10H15NO3/c1-2-13-10(12)5-6-11-8-9-4-3-7-14-9/h3-4,7,11H,2,5-6,8H2,1H3
InChI key:InChIKey=CUWYCUOEHDOVAJ-UHFFFAOYSA-N
SMILES:C(NCCC(OCC)=O)C1=CC=CO1
Synonyms:
  • 3-[[(Furan-2-yl)methyl]amino]propionic acid ethyl ester
  • N-(2-Furanylmethyl)-β-alanine ethyl ester
  • ethyl N-(furan-2-ylmethyl)-beta-alaninate
  • β-Alanine, N-(2-furanylmethyl)-, ethyl ester
  • Ethyl 3-[(fur-2-ylmethyl)amino]propanoate 97%
  • Ethyl3-[(fur-2-ylmethyl)amino]propanoate97%
  • ethyl 3-{[(furan-2-yl)methyl]amino}propanoate
  • ETHYL 3-[(2-FURYLMETHYL)AMINO]PROPANOATE
  • ETHYL 3-(FURFURYLAMINO)PROPIONATE
  • BUTTPARK 32\04-14
  • Ethyl 3-[(fur-2-ylmethyl)amino]propanoate
Sort by

Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 2 products.