92929-51-6

Basic information

• Product Name: 1-Naphthalenol, 4-nitro-, benzoate (ester)
• CAS NO: 92929-51-6
• Molecular Formula: C17H11NO4
• Molecular Weight: 293.279
• Mol File: 92929-51-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-Naphthalenol, 4-nitro-, benzoate (ester)(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Naphthalenol, 4-nitro-, benzoate (ester)(92929-51-6)
• EPA Substance Registry System: 1-Naphthalenol, 4-nitro-, benzoate (ester)(92929-51-6)

Safety Data

• Hazardous Substances Data: 92929-51-6(Hazardous Substances Data)

Upstream product

• 607-55-6 α-naphthyl benzoate 
• 607-58-9 1-(phenylmethoxy)naphthalene 
• 605-62-9 4-nitro-1-naphthol 
• 98-88-4 benzoyl chloride 
• 86-57-7 1-Nitronaphthalene 
• 94-36-0 dibenzoyl peroxide 

Downstream Products

• 5410-72-0 benzoic acid-(4-amino-[1]naphthyl ester) 

Relevant articles and documents

Regioselective Functionalization of Alkyl Aryl Ethers

A new procedure for regioselective functionalization of sensitive alkyl aryl ethers has been proposed as an alternative to picrate and sulphonamide derivatives.The procedure is based upon their reaction with cerium(IV) ammonium nitrate (CAN) and gives good yields of nitro substituted ethers, affording one pot synthesis of hitherto unknown 1-isopropoxy-4-nitronaphthalene, 1-butoxy-4-nitronaphthalene, 2-isopropoxy-6-nitronaphthalene and 2-butoxy-6-nitronaphthalene.A plausible mechanism has been suggested.

Oxidative Derivatisation of Aromatic Ethers

Reaction of cerium(IV) ammonium nitrate with some naphthyl ethers has been studied as a substitute to traditionally used hydrolytic cleavage method for their identification.One-pot, one-step synthesis of 2,2'-dinitro-1,1'-diethoxy-4,4'-bisnaphthalene; 2,2'-diethoxy-8-nitro-4,4'-bisnaphthalene; 1,8-dinitro-2-methoxynaphthalene; 2-methoxy-8-nitronaphthalene; 1-methoxy-4-nitronaphthalene; 1-ethoxy-4-nitronaphthalene; 4-nitro-1-naphthylbenzoate; 2-methoxy-6-nitronaphthalene; 1-nitro-2-naphthylbenzoate are described.