1258239-63-2

Basic information

• Product Name: N'-tert-butyl-N-4-(ethoxycarbonyl)phenyl carbodiimide
• Synonyms: N'-tert-butyl-N-4-(ethoxycarbonyl)phenyl carbodiimide
• CAS NO: 1258239-63-2
• Molecular Weight: 246.309
• Mol File: 1258239-63-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N'-tert-butyl-N-4-(ethoxycarbonyl)phenyl carbodiimide(CAS DataBase Reference)
• NIST Chemistry Reference: N'-tert-butyl-N-4-(ethoxycarbonyl)phenyl carbodiimide(1258239-63-2)
• EPA Substance Registry System: N'-tert-butyl-N-4-(ethoxycarbonyl)phenyl carbodiimide(1258239-63-2)

Safety Data

• Hazardous Substances Data: 1258239-63-2(Hazardous Substances Data)

Upstream product

• 119072-55-8 tert-butylisonitrile 
• 38556-93-3 4-azido-benzoic acid ethyl ester 
• 94-09-7 p-aminoethylbenzoate 
• 190712-80-2 TiCl₂(N-tert-butylimido)bischlorobis(pyridine)titanium(IV) 
• 30806-83-8 p-ethoxycarbonylphenyl isocyanate 

Downstream Products

• 890365-88-5 N'-tert-butyl-N-4-ethoxycarbonylphenyl urea 

Relevant articles and documents

Synthesis of carbodiimides by I2/CHP-mediated cross-coupling reaction of isocyanides with amines under metal-free conditions

An I2/CHP-mediated cross-coupling reaction of isocyanides with readily accessible amines via C-N formation is described for carbodiimide synthesis in moderate to excellent yields. This represents a metal-free strategy for a coupling reaction of isocyanides with amines, and it provides an efficient approach for symmetric and unsymmetric functionalized carbodiimide derivative synthesis under mild conditions.

The efficient synthesis of carbodiimides using a titanium imido complex

An efficient rt synthesis of carbodiimides or ureas from the combination of a titanium imido complex 2 and a range of 12 aryl and aliphatic isocyanates is described. Control experiments suggest that carbodimide formation is via heterocumulene metathesis t