2437-30-1

Basic information

• Product Name: N-(2-nitronaphthalen-1-yl)acetamide
• CAS NO: 2437-30-1
• Molecular Formula: C₁₂H₁₀N₂O₃
• Molecular Weight: 230.2194
• Mol File: 2437-30-1.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 485.6°C at 760 mmHg
• Flash Point: 247.5°C
• Density: 1.366g/cm³
• Vapor Pressure: 1.39E-09mmHg at 25°C
• Refractive Index: 1.697
• CAS DataBase Reference: N-(2-nitronaphthalen-1-yl)acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-nitronaphthalen-1-yl)acetamide(2437-30-1)
• EPA Substance Registry System: N-(2-nitronaphthalen-1-yl)acetamide(2437-30-1)

Safety Data

• Hazardous Substances Data: 2437-30-1(Hazardous Substances Data)

Upstream product

• 607-23-8 2-nitro-1-naphthylamine 
• 108-24-7 acetic anhydride 
• 575-36-0 1-acetamidonaphthalene 
• 7697-37-2 nitric acid 
• 64-19-7 acetic acid 
• 57-13-6 urea 
• 134-32-7 1-amino-naphthalene 
• 7664-41-7 ammonia 

Downstream Products

• 7499-73-2 N-(4-bromo-2-nitronaphthalen-1-yl)acetamide 
• 607-24-9 2-nitro-1-naphthol 
• 607-23-8 2-nitro-1-naphthylamine 
• 1792-42-3 2-methyl-1H-naphth[1,2-d]imidazole 
• 90799-46-5 4-chloro-2-naphthylamine 
• 53526-29-7 1-chloro-3-nitronaphthalene 

Relevant articles and documents

Regioselective ortho-nitration of N-phenyl carboxamides and primary anilines using bismuth nitrate/acetic anhydride

An efficient and one-pot synthetic method for the regioselective ortho-nitration of the N-phenyl carboxamides and primary anilines has been developed by using bismuth nitrate and acetic anhydride as the nitrating reagents. Reaction proceeds at room temperature and results in corresponding ortho-nitrated products in moderate to excellent yields. This method provides an operationally simple, regioselective, and efficient access to synthesize o-nitro anilines under the mild conditions.