CAS 10250-66-5: 3-[(ANILINOCARBONYL)AMINO]PROPANOIC ACID

Description: 3-[(Anilinocarbonyl)amino]propanoic acid, with the CAS number 10250-66-5, is an organic compound characterized by its structure, which includes an aniline moiety linked to a propanoic acid backbone through a carbonyl and amino group. This compound typically exhibits properties associated with both amino acids and aromatic amines, including potential solubility in polar solvents due to the presence of the carboxylic acid group. It may participate in various chemical reactions, such as amide formation and coupling reactions, owing to its functional groups. The presence of the aniline group suggests that it may exhibit basic properties and can engage in hydrogen bonding, influencing its reactivity and interactions with other molecules. Additionally, this compound may have applications in pharmaceuticals or as a building block in organic synthesis, given its structural features that allow for further functionalization. Its stability and reactivity can be influenced by environmental factors such as pH and temperature, which are important considerations in its handling and application.

Formula: C₁₀H₁₁N₂O₃

InChI: InChI=1/C10H12N2O3/c13-9(14)6-7-11-10(15)12-8-4-2-1-3-5-8/h1-5H,6-7H2,(H,13,14)(H2,11,12,15)/p-1

Synonyms:

• N-(phenylcarbamoyl)-beta-alanine
• 3-[(Phenylcarbamoyl)Amino]Propanoate

β-Alanine, N-[(phenylamino)carbonyl]-

CAS: 10250-66-5

• Formula: C₁₀H₁₂N₂O₃
• Molecular weight: 208.2139

3-[(Phenylcarbamoyl)amino]propanoic acid

CAS: 10250-66-5

Versatile small molecule scaffold

• Formula: C₁₀H₁₂N₂O₃
• Purity: Min. 95%
• Molecular weight: 208.21 g/mol

3-[(phenylcarbamoyl)amino]propanoic acid

CAS: 10250-66-5

• Purity: 97%
• Molecular weight: 208.2169952392578