6285-85-4

Basic information

• Product Name: 2-amino-5-methoxy-2,3-dihydro-1H-inden-1-one
• CAS NO: 6285-85-4
• Molecular Formula: C₁₀H₁₁NO₂
• Molecular Weight: 177.1998
• Mol File: 6285-85-4.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 342.9°C at 760 mmHg
• Flash Point: 187.7°C
• Density: 1.208g/cm³
• Vapor Pressure: 7.28E-05mmHg at 25°C
• Refractive Index: 1.58
• CAS DataBase Reference: 2-amino-5-methoxy-2,3-dihydro-1H-inden-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 2-amino-5-methoxy-2,3-dihydro-1H-inden-1-one(6285-85-4)
• EPA Substance Registry System: 2-amino-5-methoxy-2,3-dihydro-1H-inden-1-one(6285-85-4)

Safety Data

• Hazardous Substances Data: 6285-85-4(Hazardous Substances Data)

Usage

Chemical compound

2-amino-5-methoxy-2,3-dihydro-1H-inden-1-one

Contains

amino group and methoxy group

Potential pharmacological applications

anti-inflammatory, anti-tumor agent

Studied effects

on nervous system

Potential applications

treatment of neurological disorders
Further research needed to fully understand properties and potential uses

Upstream product

• 5111-70-6 5-methoxy-1-indanone 
• 7235-36-1 5-methoxy-indan-1,2-dione 2-oxime 

Relevant articles and documents

Squaramide-catalysed asymmetric Michael addition/cyclization cascade reaction of 4-arylmethylidene-2,3-dioxopyrrolidines with 2-isothiocyanato-1-indanones

A highly efficient cinchona alkaloid-derived squaramide catalysed asymmetric Michael/cyclization cascade reaction of 4-arylmethylidene-2,3-dioxopyrrolidines with 2-isothiocyanato-1-indanones was successfully developed. This protocol provides an efficient

Syntheses and Photophysical Properties of Some 5(2)-Aryl-2(5)-(4-pyridyl)oxazoles and Related Oxadiazoles and Furans

A number of 5-aryl-2-(4-pyridyl)oxazoles, a 2-aryl-5-(4-pyridyl)oxazole, the related oxadiazole and furan, several 2-(4-pyridyl)cycloalkanooxazoles, and many of their quaternary salts were prepared.No single standard synthesis was effective for preparation of more than a few of the 25 free bases described; methods often unique to a base were employed.Minor variations in structure sometimes produced large differences in absorption and emission wavelengths, as well as in the magnitude of the extinction coefficient.The salts are of interest as laser dyes, scintillation fluors, biological stains, and shifters for luminescent solar concentrators.