78158-32-4

Basic information

• Product Name: Acetamide, 2-bromo-N-(phenylmethoxy)-
• CAS NO: 78158-32-4
• Molecular Formula: C9H10BrNO2
• Molecular Weight: 244.088
• Mol File: 78158-32-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Acetamide, 2-bromo-N-(phenylmethoxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: Acetamide, 2-bromo-N-(phenylmethoxy)-(78158-32-4)
• EPA Substance Registry System: Acetamide, 2-bromo-N-(phenylmethoxy)-(78158-32-4)

Safety Data

• Hazardous Substances Data: 78158-32-4(Hazardous Substances Data)

Upstream product

• 622-33-3 N-benzyloxyamine 
• 2687-43-6 O-benzylhydoxylamine hydrochloride 
• 598-21-0 2-Bromoacetyl bromide 

Relevant articles and documents

Z-2-(2-acyl methylene) thiazolidine-4-ketone derivative as well as preparation method and application thereof

The invention relates to the field of chemical synthesis, in particular to Z-2-(2-acyl methylene) thiazolidine-4-ketone derivatives as well as a preparation method and application thereof. The structural formula of the Z-2-(2-acyl methylene) thiazolidine-

Regio- and Diastereoselective Access to 4-Imidazolidinones via an Aza-Mannich Initiated Cyclization of Sulfamate-Derived Cyclic Imines with α-Halo Hydroxamates

An efficient regio- and diastereoselective cyclization of sulfamate-derived cyclic imines with unsubstituted or monosubstituted α-halo hydroxamates is developed under mild conditions. This reaction proceeds smoothly under transition-metal-free conditions via a domino aza-Mannich addition/intramolecular nucleophilic substitution sequence, providing a convenient route to access 2-monosubstituted and 2,5-disubstituted 4-imidazolidinones. Notably, the products were obtained with single trans-isomers in moderate to excellent yields.