2-Acetamidoacrylic acid

CAS: 5429-56-1

Ref. 3D-FA16936

Produktinformation

• Name: 2-Acetamidoacrylic acid
• Synonyme: 2-(Acetylamino)-2-propenoic acid2-(Acetylamino)acrylic acidAcetyldehydroalanine, 2-(Acetylamino)-2-propenoic acid, 2-(Acetylamino)Prop-2-Enoate, 2-(Acetylamino)Prop-2-Enoic Acid, 2-(Acetylamino)acrylic acid, 2-Acetamidoprop-2-enoic acid, 2-Propenoic acid, 2-(acetylamino)-, Ac-DL-Dha-OH~N-Acetyldehydroalanine, Acetyldehydroalanine, Acrylic acid, 2-acetamido-, N-Acetyl-α,β-dehydroalanine, N-Acetyl-α-aminoacrylic acid, N-Acetyldehydroalanine, NSC 14171, α-(Acetylamino)acrylic acid, α-Acetamidoacrylic acid

Beschreibung

2-Acetamidoacrylic acid is an organic compound that belongs to the class of trifluoroacetic acids. It has been shown to have a photoelectron spectrum with a maximum at 9.5 eV, which corresponds to the sodium salt form. This acid has also been found in a kinetic study to be hydrolyzed by amines and malonic acid, and bacterial translocation studies have shown that it can inhibit the transport of bacteria across epithelial barriers. 2-Acetamidoacrylic acid is used as a reagent for the preparation of sodium carbonate from sodium salts and carbon dioxide, and can be converted into acrylamide by heating with ammonia gas or ammonium hydroxide solution. The conformational properties of this molecule are determined by its reactivity with water, which leads to the formation of hydrogen bonds. 2-Acetamidoacrylic acid has also been shown to activate tumor cells through antibody binding, leading to an antit

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 129.11 g/mol
• Formel: C₅H₇NO₃
• Reinheit: Min. 95%
• InChl: InChI=1S/C5H7NO3/c1-3(5(8)9)6-4(2)7/h1H2,2H3,(H,6,7)(H,8,9)
• InChI Key: InChIKey=UFDFFEMHDKXMBG-UHFFFAOYSA-N
• SMILES: C=C(NC(C)=O)C(=O)O