848170-22-9

Basic information

• Product Name: N-METHOXY-N-METHYL-2,3-DIHYDROBENZO[B][1,4]DIOXINE-2-CARBOXAMIDE
• Synonyms: N-METHOXY-N-METHYL-2,3-DIHYDROBENZO[B][1,4]DIOXINE-2-CARBOXAMIDE;N-Methoxy-N-methyl-2,3-dihydro-benzo[1,4]dioxine-2-carboxamide;1,4-Benzodioxin-2-carboxamide, 2,3-dihydro-N-methoxy-N-methyl-
• CAS NO: 848170-22-9
• Molecular Formula: C11H13 N O4
• Molecular Weight: 223.23
• Mol File: 848170-22-9.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-METHOXY-N-METHYL-2,3-DIHYDROBENZO[B][1,4]DIOXINE-2-CARBOXAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: N-METHOXY-N-METHYL-2,3-DIHYDROBENZO[B][1,4]DIOXINE-2-CARBOXAMIDE(848170-22-9)
• EPA Substance Registry System: N-METHOXY-N-METHYL-2,3-DIHYDROBENZO[B][1,4]DIOXINE-2-CARBOXAMIDE(848170-22-9)

Safety Data

• Hazardous Substances Data: 848170-22-9(Hazardous Substances Data)

Usage

General Description

N-Methoxy-N-methyl-2,3-dihydrobenzo[b][1,4]dioxine-2-carboxamide is a compound with a chemical formula C11H13NO3. It belongs to the class of amides and contains a benzodioxane moiety. This chemical may have potential uses in the pharmaceutical industry, particularly in the development of new drugs or medications. Its specific properties and potential applications would depend on further research and testing.

Upstream product

• 3663-80-7 1,4-benzodioxane-2-carboxylic acid 
• 6638-79-5 N,O-dimethylhydroxylamine*hydrochloride 
• 1246188-97-5 (2,3-dihydrobenzo[b][1,4]dioxin-2-yl)(1H-imidazol-1-yl)methanone 
• 650597-66-3 (S)‐methyl 1,4‐benzodioxane‐2‐carboxylate 

Relevant articles and documents

How do reaction conditions affect the enantiopure synthesis of 2-substituted-1,4-benzodioxane derivatives?

Several biologically active compounds structurally include the enantiopure 2-substituted-1,4-benzodioxane scaffold. The straightforward racemization that affects reactions involving most of the common chemical reactives is thus a crucial issue. The developing of a completely stereo-controlled synthetic route that does not affect the enantiomeric excess is consequently mandatory. It is also important to set up a reliable chiral HPLC method, able to follow the reaction, and to improve the synthetic performances. Here, we report the chiral investigation of two different synthons, we specifically evaluated the synthetic pathways that could be run in order to afford them, avoiding the racemization processes, which could normally occur in basic conditions. In addition, we developed peculiar chiral HPLC methods in order to resolve the enantiomers, define the enantiomeric excess, and fully characterize these compounds.