14046-88-9

Basic information

• Product Name: 3-(2-Aminoethyl)-5,5-diphenylhydantoin
• Synonyms: 3-(2-Aminoethyl)-5,5-diphenylhydantoin
• CAS NO: 14046-88-9
• Molecular Formula: C₁₇H₁₇N₃O₂
• Molecular Weight: 0
• Mol File: 14046-88-9.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3-(2-Aminoethyl)-5,5-diphenylhydantoin(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(2-Aminoethyl)-5,5-diphenylhydantoin(14046-88-9)
• EPA Substance Registry System: 3-(2-Aminoethyl)-5,5-diphenylhydantoin(14046-88-9)

Safety Data

• Hazardous Substances Data: 14046-88-9(Hazardous Substances Data)

Upstream product

• 20000-09-3 3-(2'-phthalimidoethyl)-5,5-diphenylhydantoin 
• 151-56-4 ethyleneimine 
• 57-41-0 phenythoin 

Downstream Products

• 92220-76-3 N-<2-(5,5-diphenyl-2,4-imidazolidinedion-3-yl)ethyl>-7-acetoxy-1-naphthalene sulfonamide 
• 92241-06-0 2-8-phenytoin 

Relevant articles and documents

Nucleophilic ring opening of aziridines

This account of research work on nucleophilic ring opening (NRO) of aziridines (Az's) demonstrates the broad synthetic scope of this reaction, inclusive secondary reactions, and it discusses the special mechanistic fundamentals and details as well as mechanistic variants. Formation of a C-C bond by NRO is the red thread in this report. A central mechanistic aspect is the quality of the leaving group in Az bases, aziridinium ions and activated Az's (acyl, sulfonyl; double activation). Factors controlling the regioselectivity of NRO are dealt with as well as the influence of the nitrogen pyramid. Competing reactions include carbonyl attack (acylated Az's) and electron transfer with cases of pseudo-NRO (multistep radical paths). Wiley-VCH Verlag GmbH, 1999.