1354028-34-4

Basic information

• Product Name: (2,3-Dihydro-benzo[1,4]dioxin-2-yl)-((R)-3-hydroxy-pyrrolidin-1-yl)-Methanone
• Synonyms: (2,3-Dihydro-benzo[1,4]dioxin-2-yl)-((R)-3-hydroxy-pyrrolidin-1-yl)-Methanone;(2,3-Dihydrobenzo[b][1,4]dioxin-2-yl)((R)-3-hydroxypyrrolidin-1-yl)Methanone
• CAS NO: 1354028-34-4
• Molecular Formula: C13H15NO4
• Molecular Weight: 249.2625
• Mol File: 1354028-34-4.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (2,3-Dihydro-benzo[1,4]dioxin-2-yl)-((R)-3-hydroxy-pyrrolidin-1-yl)-Methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (2,3-Dihydro-benzo[1,4]dioxin-2-yl)-((R)-3-hydroxy-pyrrolidin-1-yl)-Methanone(1354028-34-4)
• EPA Substance Registry System: (2,3-Dihydro-benzo[1,4]dioxin-2-yl)-((R)-3-hydroxy-pyrrolidin-1-yl)-Methanone(1354028-34-4)

Safety Data

• Hazardous Substances Data: 1354028-34-4(Hazardous Substances Data)

Usage

Description

(2,3-Dihydro-benzo[1,4]dioxin-2-yl)-((R)-3-hydroxy-pyrrolidin-1-yl)-Methanone is a complex organic molecule featuring a benzo[1,4]dioxin ring fused with a hydroxy-pyrrolidinyl-methanone group. As a chiral molecule, its stereochemistry is determined by the (R)-3-hydroxy-pyrrolidin-1-yl group. The structural elements present in this compound hint at possible pharmaceutical or biological activity, as similar motifs are prevalent in many biologically active substances. Further investigation is required to ascertain its specific characteristics and potential applications.

Uses

Used in Pharmaceutical Industry:
(2,3-Dihydro-benzo[1,4]dioxin-2-yl)-((R)-3-hydroxy-pyrrolidin-1-yl)-Methanone is used as a potential pharmaceutical agent due to its complex structure and the presence of biologically active motifs, which may contribute to its efficacy in treating various medical conditions.
Used in Research and Development:
In the field of organic chemistry and medicinal chemistry, (2,3-Dihydro-benzo[1,4]dioxin-2-yl)-((R)-3-hydroxy-pyrrolidin-1-yl)-Methanone serves as a subject for research and development. Its unique structure and chirality make it an interesting candidate for studies aimed at understanding its properties, reactivity, and potential applications in drug discovery and design.