154374-54-6

Basic information

• Product Name: N-(4-methoxy-benzoyl)-N'-(4-methoxy-phenyl)-urea
• Synonyms: N-(4-methoxy-benzoyl)-N'-(4-methoxy-phenyl)-urea
• CAS NO: 154374-54-6
• Molecular Weight: 300.314
• Mol File: 154374-54-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-(4-methoxy-benzoyl)-N'-(4-methoxy-phenyl)-urea(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-methoxy-benzoyl)-N'-(4-methoxy-phenyl)-urea(154374-54-6)
• EPA Substance Registry System: N-(4-methoxy-benzoyl)-N'-(4-methoxy-phenyl)-urea(154374-54-6)

Safety Data

• Hazardous Substances Data: 154374-54-6(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 3424-93-9 4-methoxyphenylacetamide 
• 7726-95-6 bromine 
• 124-41-4 sodium methylate 

Downstream Products

• 123-30-8 4-amino-phenol 
• 99-96-7 4-hydroxy-benzoic acid 

Relevant articles and documents

In situ slow release of isocyanates: Synthesis and organocatalytic application of N-acylureas

A novel, efficient, and operationally simple one-pot synthesis of both, symmetrical and unsymmetrical N-acylureas from carboxamides and in situ generated isocyanates (from N,N-dibromo-p-toluenesulfonamide) in the presence of a mild base at rt is reported. The protocol avoids the tedious isolation and purification steps of hazardous isocyanates. The first application of these acylureas to the catalysis through hydrogen bonding is also demonstrated.