29900-75-2

Basic information

• Product Name: 2-Propenamide, N-hydroxy-3-phenyl-, (2E)-
• CAS NO: 29900-75-2
• Molecular Formula: C9H9NO2
• Molecular Weight: 163.176
• Mol File: 29900-75-2.mol
• Article Data: 17

Chemical Properties

• CAS DataBase Reference: 2-Propenamide, N-hydroxy-3-phenyl-, (2E)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propenamide, N-hydroxy-3-phenyl-, (2E)-(29900-75-2)
• EPA Substance Registry System: 2-Propenamide, N-hydroxy-3-phenyl-, (2E)-(29900-75-2)

Safety Data

• Hazardous Substances Data: 29900-75-2(Hazardous Substances Data)

Upstream product

• 4192-77-2 ethyl cinnamate 
• 140-10-3 (E)-3-phenylacrylic acid 
• 1138-15-4 cinnamoyl imidazole 
• 102-92-1 Cinnamoyl chloride 
• 23776-87-6 2,5‐dioxopyrrolidin‐1‐yl cinnamate 
• 1426580-48-4 N-(2,3-dimethylbut-2-enyloxy)cinnamamide 
• 14371-10-9 (E)-3-phenylpropenal 
• 103-26-4 Methyl cinnamate 

Downstream Products

• 33934-11-1 N-Methyl-3-phenylisoxazolidine-5-one 
• 1885-38-7 cinnamic nitrile 
• 107487-07-0 (E)-5-phenyl-3-(2-phenylethenyl)-2-isoxazoline 
• 4192-77-2 ethyl cinnamate 
• 56735-73-0 N-hydroxy-N-morpholin-4-ylmethyl-3-phenyl-acrylamide 

Relevant articles and documents

Cosmetic preservative and application thereof as cosmetic formula component

The invention relates to the field of preservatives, in particular to a cosmetic preservative which comprises any one of the general I, or two or more compounds, wherein R1 represents H, OH, methyl, methoxy, F, Cl or Br. Herein, R2 is H represented Na by

An Environmentally Sustainable Mechanochemical Route to Hydroxamic Acid Derivatives

An operationally simple, and cost efficient conversion of carboxylic acids into hydroxamic acid derivatives via a high-energy mechanochemical activation is presented. This ball milling methodology was applied to a wide variety of carboxylic acids dramatically improving purification issues associated with this class of molecules, which still remain one of the main bottlenecks of classical methodologies. (Figure presented.).

Dioxazoles, a new mild nitrene transfer reagent in gold catalysis: Highly efficient synthesis of functionalized oxazoles

A gold-catalyzed regioselective [3+2] cycloaddition of ynamides with 1,4,2-dioxazoles was developed and offers a novel approach to obtain highly functionalized oxazoles under mild reaction conditions. 1,4,2-Dioxazole was found to act as an efficient N-acyl nitrene equivalent to trigger a facile generation of α-imino gold-carbene intermediate through the elimination of a ketone.