CAS 102-01-2: Acetoacetanilide
Formula:C10H11NO2
InChI:InChI=1S/C10H11NO2/c1-8(12)7-10(13)11-9-5-3-2-4-6-9/h2-6H,7H2,1H3,(H,11,13)
InChI key:InChIKey=DYRDKSSFIWVSNM-UHFFFAOYSA-N
SMILES:N(C(CC(C)=O)=O)C1=CC=CC=C1
Synonyms:- 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
- See more synonyms
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Found 7 products.
Acetoacetanilide, 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 Scientific Chemicals.Formula:C10H11NO2Purity:98+%Color and Shape:White to pale cream or pale grey, Crystals or powder or crystalline powderMolecular weight:177.20Acetoacetanilide, 99%
CAS:This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product portfolio. Some documentation and label information may refer to the legacy brand. The original Acros Organics product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.Formula:C10H11NO2Purity:99%Color and Shape:Powder or crystals, WhiteMolecular weight:177.20Acetoacetanilide
CAS:Formula:C10H11NO2Purity:>99.0%(HPLC)(N)Color and Shape:White to Almost white powder to crystalMolecular weight:177.20Acetoacetanilide
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.Purity:Min. 95%
