(S)-2-Amino-3-(furan-3-yl)propanoic acid

Base Information

• Chemical Name: (S)-2-Amino-3-(furan-3-yl)propanoic acid
• CAS No.: 129030-32-6
• Molecular Formula: C₇H₉NO₃
• Molecular Weight: 155.153
• DSSTox Substance ID: DTXSID20564174
• Nikkaji Number: J1.507.683F
• Mol file: 129030-32-6.mol

Synonyms:(S)-2-Amino-3-(furan-3-yl)propanoic acid;129030-32-6;(2S)-2-AMINO-3-(FURAN-3-YL)PROPANOIC ACID;3-(3-Furyl)-L-alanine;3-Furanpropanoic acid, alpha-amino-, (S)- (9CI);beta-3-furylalanine;(S)-2-Amino-3-(furan-3-yl)propanoicacid;3-Furan-3-yl-L-alanine;SCHEMBL537569;DTXSID20564174;AKOS012506779;CS-0270964;EN300-1299971;A933790

Chemical Property of (S)-2-Amino-3-(furan-3-yl)propanoic acid

Chemical Property:

• XLogP3: -2.3
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 3
• Exact Mass: 155.058243149
• Heavy Atom Count: 11
• Complexity: 149

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=COC=C1CC(C(=O)O)N
• Isomeric SMILES: C1=COC=C1C[C@@H](C(=O)O)N
• Use Description: (S)-2-Amino-3-(furan-3-yl)propanoic acid, also known as L-Furafylline, has diverse applications in different fields. In the realm of pharmaceuticals and medicine, it plays a crucial role as a chemical intermediate and research tool. Its derivatives are investigated for their potential therapeutic applications, particularly in the treatment of respiratory diseases like asthma and chronic obstructive pulmonary disease (COPD). Additionally, in the field of organic chemistry, it can be employed as a chiral building block for the synthesis of complex organic molecules and pharmaceutical compounds. Furthermore, (S)-2-Amino-3-(furan-3-yl)propanoic acid has applications in biochemical research, serving as a reference compound and research probe for studying enzymes, such as cytochrome P450, and their interactions with drugs. Its multifaceted utility underscores its significance in drug development, chemical synthesis, and biochemical investigations, where it plays essential roles in advancing scientific research and the development of novel pharmaceuticals.