312488-22-5

Basic information

• Product Name: C₁₀H₁₃NO
• Synonyms: C₁₀H₁₃NO
• CAS NO: 312488-22-5
• Molecular Weight: 163.219
• Mol File: 312488-22-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₁₀H₁₃NO(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₀H₁₃NO(312488-22-5)
• EPA Substance Registry System: C₁₀H₁₃NO(312488-22-5)

Safety Data

• Hazardous Substances Data: 312488-22-5(Hazardous Substances Data)

Upstream product

• 24549-06-2 6-ethyl-o-toluidine 
• 2258-42-6 formyl acetic anhydride 

Downstream Products

• 21548-51-6 2-ethyl-6-methylphenylisocyanide 
• 102705-32-8 7-ethyl-2-phenyl-1H-indole 

Relevant articles and documents

Synthesis of sugar-derived isoselenocyanates, selenoureas, and selenazoles

Aryl, alkyl, and sugar-derived isoselenocyanates were prepared by a one-pot procedure starting from the corresponding formamides, using triphosgene as a dehydrating agent, triethylamine, and black selenium powder. The preparation of sugar selenoureas by coupling of O-protected sugar-derived isoselenocyanates with different amines, and by coupling of unprotected glycopyranosyl amines with phenyl isoselenocyanate was also accomplished. The synthesis of a glucopyranos-2-yl-selenazole starting from O-protected 2-amino-2-deoxy-d-glucose by coupling with benzoyl isoselenocyanate, Se-alkylation with phenacyl bromide, and acid-catalyzed dehydration is also reported. Unprotected N-(β-d-glucopyranosyl)-N′-phenylselenourea was transformed into a 1,2-trans-fused bicyclic isourea upon treatment with aqueous hydrogen peroxide; the same isourea was prepared by a one-pot three-step procedure from β-d-glycopyranosylamine by thiophosgenation, coupling with aniline, and HgO-mediated desulfurization.