622403-42-3

Basic information

• Product Name: 1-phenyl-3-(2-ethoxycarbonylphenyl) carbodiimide
• Synonyms: 1-phenyl-3-(2-ethoxycarbonylphenyl) carbodiimide
• CAS NO: 622403-42-3
• Molecular Weight: 266.299
• Mol File: 622403-42-3.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: 1-phenyl-3-(2-ethoxycarbonylphenyl) carbodiimide(CAS DataBase Reference)
• NIST Chemistry Reference: 1-phenyl-3-(2-ethoxycarbonylphenyl) carbodiimide(622403-42-3)
• EPA Substance Registry System: 1-phenyl-3-(2-ethoxycarbonylphenyl) carbodiimide(622403-42-3)

Safety Data

• Hazardous Substances Data: 622403-42-3(Hazardous Substances Data)

Upstream product

• 118-92-3 anthranilic acid 
• 103-72-0 phenyl isothiocyanate 
• 179039-70-4 ethyl 2-(triphenylphosphoranylidene-amino)benzoate 
• 90408-05-2 o-azidobenzoic acid ethyl ester 
• 32045-49-1 ethyl-o-aminobenzoate hydrochloride 
• 31162-13-7 2-azidobenzoic acid 
• 103-71-9 phenyl isocyanate 

Downstream Products

• 741-75-3 2-(piperidin-1-yl)-3-phenylquinazolin-4(3H)-one 
• 741-76-4 2-(morpholin-4-yl)-3-phenylquinazolin-4(3H)-one 
• 1078626-29-5 C₃₄H₃₂N₆O₄ 
• 1078626-03-5 3-aminoethyl-2-anilino-quinazoline-4(3Η)-one 
• 1078626-17-1 C₃₀H₂₄N₆O₂ 
• 1078626-20-6 C₃₁H₂₆N₆O₂ 
• 1078626-06-8 3-aminopropyl-2-anilino-quinazoline-4(3Η)-one 
• 1078626-24-0 C₃₁H₂₆N₆O₂ 
• 1078626-27-3 C₃₂H₂₈N₆O₂ 
• 5260-41-3 2-ethyl-3-phenyl-3H-quinazolin-4-one 
• 22686-82-4 2,3-diphenyl-3H-quinazolin-4-one 
• 1414871-28-5 2-cyclohexyl-3-phenylquinazolin-4(3H)-one 
• 1189261-10-6 2-ethenyl-3-phenylquinazolin-4(3H)-one 
• 2385-23-1 2-Methyl-3-phenyl-4(3H)-quinazolinone 

Relevant articles and documents

New efficient synthesis of 2-aryloxy-4(3H)-quinazolinones

2-Aryloxy-4(3H)-quinazolinones 5 were synthesized from cyclization of carbodiimides 2 with various phenols in presence of catalytic solid potassium carbonate in satisfactory yields.

Novel 4(3H)-Quinazolinone Derivatives Containing an Isoxazole Moiety: Design, Synthesis, and Bioactivity Evaluation

The aim of the present study is to design and synthesize a series of novel 4(3H)-quinazolinone derivatives containing an isoxazole moiety and evaluate their antifungal activity against Gibberella zeae (G. zeae), Fusarium oxysporum (F. oxysporum), Cytospor

Functionalized carbodiimide mediated synthesis of 2,3-disubstituted quinazolin-4(3 H)-ones via the tandem strategy of C-nucleophilic addition and intramolecular NH-substitution cyclization

A facile synthesis of quinazolin-4(3H)-ones possessing carbon substituents at positions 2 and 3 has been developed. Key to the synthesis is a tandem strategy involving introduction of a 2-substituent and construction of the quinazolinone framework via C-nucleophilic addition to the carbodiimide cumulenic carbon followed by intramolecular nucleophilic substitution by the newly formed NH moiety at the proximal ester group.