75510-87-1

Basic information

• Product Name: Naphth[1,2-d]oxazole, 2-(4-methoxyphenyl)-
• CAS NO: 75510-87-1
• Molecular Formula: C18H13NO2
• Molecular Weight: 275.307
• Mol File: 75510-87-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Naphth[1,2-d]oxazole, 2-(4-methoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Naphth[1,2-d]oxazole, 2-(4-methoxyphenyl)-(75510-87-1)
• EPA Substance Registry System: Naphth[1,2-d]oxazole, 2-(4-methoxyphenyl)-(75510-87-1)

Safety Data

• Hazardous Substances Data: 75510-87-1(Hazardous Substances Data)

Upstream product

• 2746-25-0 p-Methoxybenzyl bromide 
• 131-91-9 1-Nitroso-2-naphthol 
• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 5720-07-0 4-methoxyphenylboronic acid 
• 233-70-5 naphtho[1,2-d]oxazole 
• 2632-13-5 2-Bromo-4'-methoxyacetophenone 

Relevant articles and documents

Microwave-assisted synthesis of 2-substituted naphtho[1,2-d][1,3]oxazoles by reacting 1-nitroso-2-naphthol with allyl bromides and benzyl bromides using FeCl3 as catalyst

Efficient and improved preparation of 2-substituted[1,2-d][1,3]oxazoles by the reaction of 1-nitroso-2-naphthol and allyl bromides, benzyl bromides under microwave condition utilizing FeCl3 as a catalyst with yield ranging from 32% to 72%. Reaction with bromo acetonitrile yields the corresponding 2-cyanonaphthoxazole with 58% yield.

Reaction of 1-nitroso-2-naphthols with α-functionalized ketones and related compounds: The unexpected formation of decarbonylated 2-substituted naphtho[1,2-d][1,3]oxazoles

Reactions between 1-nitroso-2-naphthols and α-functionalized ketones such as α-bromo-, α-chloro-, α-mesyloxy-, α-tosyloxy-, and α-hydroxy ketones under basic conditions delivered 2-substituted naphtho[1,2-d][1,3]oxazoles in a single synthetic operation. T