90921-75-8

Basic information

• Product Name: 2-Ethyl-2H-benzo[b][1,4]oxazin-3(4H)-one
• Synonyms: 2-Ethyl-2H-benzo[b][1,4]oxazin-3(4H)-one;2-Ethyl-2,4-dihydro-1,4-benzoxazin-3-one;2-Ethyl-2H-1,4-benzoxazin-3(4H)-one;2-ethyl-4H-1,4-benzoxazin-3-one;2-Ethyl-4H-benzo[1,4]oxazin-3-one;BAS 07153732;2-ethyl-3,4-dihydro-2H-1,4-benzoxazin-3-one
• CAS NO: 90921-75-8
• Molecular Formula: C10H11NO2
• Molecular Weight: 177.19984
• Mol File: 90921-75-8.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2-Ethyl-2H-benzo[b][1,4]oxazin-3(4H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Ethyl-2H-benzo[b][1,4]oxazin-3(4H)-one(90921-75-8)
• EPA Substance Registry System: 2-Ethyl-2H-benzo[b][1,4]oxazin-3(4H)-one(90921-75-8)

Safety Data

• Hazardous Substances Data: 90921-75-8(Hazardous Substances Data)

Usage

General Description

2-Ethyl-2H-benzo[b][1,4]oxazin-3(4H)-one is a chemical compound with the molecular formula C11H11NO2 and a molecular weight of 189.21 g/mol. It is a heterocyclic compound containing a benzooxazine ring and an ethyl group. 2-Ethyl-2H-benzo[b][1,4]oxazin-3(4H)-one has potential applications in the pharmaceutical and agricultural industries due to its unique chemical properties. It may also have potential uses as a precursor in organic synthesis. Additionally, 2-Ethyl-2H-benzo[b][1,4]oxazin-3(4H)-one may have potential biological activities, though further research and testing are necessary to fully understand its effects.

Upstream product

• 90869-07-1 2-(2-bromo-butyrylamino)-phenol 
• 95-55-6 2-amino-phenol 
• 533-68-6 2-bromobutyric acid ethyl ester 
• 80-58-0 2-Bromobutyric acid 
• 1249621-96-2 2-(2-nitrophenoxy)butanenitrile 
• 88-75-5 2-hydroxynitrobenzene 

Downstream Products

• 52042-34-9 6-bromo-4-(2,3-dihydroxy-propyl)-2-ethyl-4H-benzo[1,4]oxazin-3-one 

Relevant articles and documents

A simple and facile route for the synthesis of 2H-1,4-benzoxazin-3-(4H)- ones via reductive cyclization of 2-(2-nitrophenoxy)acetonitrile adducts in the presence of Fe/acetic acid

A simple route for the synthesis of 1,4-benzoxazin-3-(4H)-ones is described herein. This method involves the reductive cyclization of 2-(2-nitrophenoxy) acetonitrile adducts in the presence of Fe/acetic acid in good to excellent yields. This system was compatible with various other functional groups.

Microwave-assisted one-pot regioselective synthesis of 2-alkyl-3,4-dihydro- 3-oxo-2H-1,4-benzoxazines

A protocol for regioselective one-pot synthesis of 2-alkyl-3,4-dihydro-3- oxo-2H-1,4-benzoxazines under controlled microwave heating has been developed. Starting from commercially available 2-aminophenols, a base-mediated regioselective O-alkylation took