CAS 102-01-2
:Acétoacétanilide
- 1-(2-Aminophenyl)Butane-1,3-Dione
- 1-(Phenylamino)-1,3-butanedione
- 1-(Phenylcarbamoyl)-2-propanone
- 3-Oxo-N-phenylbutyramide
- 3-oxo-N-phenylbutanamide
- 4-(Phenylamino)-2,4-butanedione
- AAA
- Aceto Acetanilide
- Acetoacetamidobenzene
- Acetoacetanilid
- Acetoacetanilida
- Acetoacetic acid anilide
- Acetoacetic anilide
- Acetoacetylanilide
- Butanamide, 3-oxo-N-phenyl-
- Coupler 633
- N-(Acetoacetyl)aniline
- N-Acetoacetanilide,2-Acetyl-acetanilide,N-(Acetylacetyl)aniline
- N-Phenyl-3-oxobutanamide
- N-Phenylacetoacetamide
- N-Phenylacetylacetamide
- Nsc 2656
- alpha-Acetylacetanilide
- α-Acetyl-N-phenylacetamide
- α-Acetylacetanilide
- β-Ketobutyranilide
- Voir plus de synonymes
Acetoacetanilide
CAS :Formule :C10H11NO2Degré de pureté :>99.0%(HPLC)(N)Couleur et forme :White to Almost white powder to crystalMasse moléculaire :177.20Acetoacetanilide, 98+%
CAS :This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci
Formule :C10H11NO2Degré de pureté :98+%Couleur et forme :White to pale cream or pale grey, Crystals or powder or crystalline powderMasse moléculaire :177.203-Oxo-N-phenylbutanamide
CAS :Formule :C10H11NO2Degré de pureté :95.0%Couleur et forme :SolidMasse moléculaire :177.203Acetoacetanilide
CAS :Produit contrôléFormule :C10H11NO2Couleur et forme :NeatMasse moléculaire :177.2Acetoacetanilide
CAS :Acetoacetanilide is an organic compound that has been used as a solvent in wastewater treatment. It is also known to have various pharmacological effects, including the suppression of autoimmune diseases, such as rheumatoid arthritis and systemic lupus erythematosus. Acetoacetanilide is a coumarin derivative with a hydroxyl group at the 2-position. It is thermodynamically stable and shows no evidence of toxicity in animal studies. Acetoacetanilide reacts quickly with sodium metal to form an anhydrous solution, which can be heated without decomposition. This reaction can be used to study hydrogen bonding between molecules. Acetoacetanilide has been shown to form stable complexes with nitrogen atoms, such as ammonia and amines, and fatty acids, such as picolinic acid and intramolecular hydrogen bonds with fatty acids.
Degré de pureté :Min. 95%





