59725-61-0

Basic information

• Product Name: 1-OXO-2,3-DIHYDRO-1H-INDEN-4-YL BENZOATE
• Synonyms: 1-OXO-2,3-DIHYDRO-1H-INDEN-4-YL BENZOATE;4-(BENZOYLOXY)-1-INDANONE;4-HYDROXY-1-INDANONE BENZOATE;1-Oxo-2,3-dihydro-1h-inden-4-yl benzoate, 95+%;4-(Benzoyloxy)-2,3-dihydro-1H-inden-1-one;Benzoic acid 1-oxoindan-4-yl ester
• CAS NO: 59725-61-0
• Molecular Formula: C₁₆H₁₂O₃
• Molecular Weight: 252.26
• Product Categories: C12 to C63;Carbonyl Compounds;Esters
• Mol File: 59725-61-0.mol
• Article Data: 3

Chemical Properties

• Melting Point: 78-82 °C(lit.)
• Boiling Point: 470℃
• Flash Point: 212℃
• Appearance: /
• Density: 1.271
• Vapor Pressure: 5.42E-09mmHg at 25°C
• Refractive Index: 1.625
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 1-OXO-2,3-DIHYDRO-1H-INDEN-4-YL BENZOATE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-OXO-2,3-DIHYDRO-1H-INDEN-4-YL BENZOATE(59725-61-0)
• EPA Substance Registry System: 1-OXO-2,3-DIHYDRO-1H-INDEN-4-YL BENZOATE(59725-61-0)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 59725-61-0(Hazardous Substances Data)

Usage

General Description

4-Hydroxy-1-indanone benzoate is an aromatic ester. It is a 4-hydroxy-2,3-dihydroinden-1-one derivative of benzoic acid.

InChI:InChI=1/C16H12O3/c17-14-10-9-13-12(14)7-4-8-15(13)19-16(18)11-5-2-1-3-6-11/h1-8H,9-10H2

Upstream product

• 59725-62-1 Benzoic acid 2-(2-chlorocarbonyl-ethyl)-phenyl ester 
• 59725-59-6 3-<2-(benzyloxy)phenyl>propionic acid 
• 119-84-6 C₆H₄(CH₂CH₂C(O)O) 
• 98-88-4 benzoyl chloride 

Downstream Products

• 40731-98-4 4-hydroxy-2,3-dihydroindan-1-one 
• 367506-67-0 benzoic acid 2,2-dihydroxy-1,3-dioxo-indan-4-yl ester 
• 367506-70-5 benzoic acid 9-oxo-9H-2-oxa-1,3,4,10-tetraazacyclopenta[b]fluoren-8-yl ester 
• 13336-31-7 4-methoxylindanone 

Relevant articles and documents

SUBSTITUTED AROMATIC CARBOXAMIDE AND UREA DERIVATIVES AS VANILLOID RECEPTOR LIGANDS

The invention relates to substituted aromatic carboxamide and urea derivatives, to processes for the preparation thereof, to pharmaceutical compositions containing these compounds and also to the use of these compounds for preparing pharmaceutical compositions (formula (I)).

Synthesis and Dopaminergic Activity of (R)- and (S)-4-Hydroxy-2-(di-n-propylamino)indan

A synthetic precursor to a potent dopaminergic agonist, (RS)-4-hydroxy-2-(di-n-propylamino)indan (1), has been resolved by classical recrystallization procedures, and the absolute configuration of the enantiomers have been established by X-ray crystallogr