15501-38-9

Basic information

• Product Name: Acetamide, N-(1,1-dimethylpropyl)-
• Synonyms: N-(1,1-dimethylpropyl)acetamide;N-tert-pentyl-acetamide;N-tert-amylacetamide;Essigsaeure-tert.-pentylamid;Acetamide,N-(1,1-dimethylpropyl);N-<1,1-Dimethyl-propyl>-acetamid;N-tert-Pentyl-acetamid;Acetyl-tert.-pentylamin
• CAS NO: 15501-38-9
• Molecular Formula: C7H15NO
• Molecular Weight: 129.202
• Mol File: 15501-38-9.mol
• Article Data: 4

Chemical Properties

• Melting Point: 77-78 °C
• Boiling Point: 209.8±8.0 °C(Predicted)
• Density: 0.860±0.06 g/cm3(Predicted)
• CAS DataBase Reference: Acetamide, N-(1,1-dimethylpropyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Acetamide, N-(1,1-dimethylpropyl)-(15501-38-9)
• EPA Substance Registry System: Acetamide, N-(1,1-dimethylpropyl)-(15501-38-9)

Safety Data

• Hazardous Substances Data: 15501-38-9(Hazardous Substances Data)

Upstream product

• 630-17-1 2,2-dimethylpropyl bromide 
• 75-05-8 acetonitrile 
• 513-35-9 2-methyl-but-2-ene 
• 75-85-4 tert-Amyl alcohol 
• 55204-72-3 Neopentyl(trimethyl)stannane 
• 3744-21-6 2,2-dimethyl-propyl 
• 107-82-4 i-pentyl bromide 
• 1808-38-4 bis(tert-butylacetyl)peroxide 
• 64-19-7 acetic acid 

Downstream Products

• 594-39-8 2-methyl-2-butylamine 

Relevant articles and documents

Ritter reactions in flow

Flow me a Ritter: Ritter reactions are performed in a simple microreactor setup using tert-butylacetate as versatile carbocation source. The protocol avoids the handling of large amounts of hot concentrated sulfuric acid as low concentrations are optimal for rapid access tert-butyl- or diphenylmethyl- protected amides. Copyright

Metal-catalyzed organic photoreactions. Photoreaction of 2-chloroacetophenone derivatives with olefins in the presence of silver trifluoromethanesulfonate

UV-irradiation of 2-chloroacetophenones and olefins in the presence of silver triflate affords naphthalenone derivatives with high regio and stereoselectivity and chemical yields. A possible mechanism is proposed.