174349-93-0

Basic information

• Product Name: 2H-INDEN-2-ONE, 5-BROMO-1,3-DIHYDRO-
• Synonyms: 2H-INDEN-2-ONE, 5-BROMO-1,3-DIHYDRO-;5-BROMO-1H-INDEN-2(3H)-ONE;5-Bromo-2-indanone;5-Bromo-1,3-dihydro-2H-inden-2-one;5-Bromoindan-2-one;2-Indanone, 5-broMo-;5-broMo-2,3-dihydro-1H-inden-2-one;5-Bromo-1,3-dihydro-2H-inden-2-one, 5-Bromo-2,3-dihydro-2-oxo-1H-indene
• CAS NO: 174349-93-0
• Molecular Formula: C₉H₇BrO
• Molecular Weight: 211.06
• Mol File: 174349-93-0.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 299.5 °C at 760 mmHg
• Flash Point: 117.2 °C
• Appearance: /
• Density: 1.608 g/cm³
• Vapor Pressure: 0.00119mmHg at 25°C
• Refractive Index: 1.622
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 2H-INDEN-2-ONE, 5-BROMO-1,3-DIHYDRO-(CAS DataBase Reference)
• NIST Chemistry Reference: 2H-INDEN-2-ONE, 5-BROMO-1,3-DIHYDRO-(174349-93-0)
• EPA Substance Registry System: 2H-INDEN-2-ONE, 5-BROMO-1,3-DIHYDRO-(174349-93-0)

Safety Data

• Hazardous Substances Data: 174349-93-0(Hazardous Substances Data)

Usage

General Description

2H-INDEN-2-ONE, 5-BROMO-1,3-DIHYDRO- is a chemical compound with the formula C9H7BrO. It is a brominated indenone derivative, which contains a bromine atom and a cyclic ketone group. 2H-INDEN-2-ONE, 5-BROMO-1,3-DIHYDRO- may have various industrial and research applications due to its unique structural and chemical properties. It is important to handle this compound with caution as it may have potential health and environmental effects if not properly managed.

InChI:InChI=1/C9H7BrO/c10-8-2-1-6-4-9(11)5-7(6)3-8/h1-3H,4-5H2

Upstream product

• 862135-61-3 5-bromo-2,3-dihydro-1H-inden-2-ol 
• 4254-29-9 indan-2-ol 
• 75476-78-7 5-bromo-1H-indene 
• 75476-86-7 6-Bromo-2,3-dihydro-1H-inden-1-ol 
• 14548-39-1 6-bromoindan-1-one 
• 1643-30-7 3-(4-bromophenyl)propionic acid 
• 862135-60-2 5-bromoindan-2-ol acetate 
• 4254-31-3 2-acetoxyindane 

Downstream Products

• 75476-78-7 5-bromo-1H-indene 
• 862135-61-3 5-bromo-2,3-dihydro-1H-inden-2-ol 

Relevant articles and documents

A kind of indan -5 - carboxamide ROR γ regulator and its use

The invention relates to a structure of formula (I) compound of formula or a stereoisomer thereof, tautomers or its pharmaceutically acceptable salt or solvate or prodrug, its preparation method, a pharmaceutical composition containing these modulators and their use in the treatment ROR γ-mediated inflammatory, metabolic and autoimmune disorders.

Daucus carota and baker's yeast mediated bio-reduction of prochiral ketones

Stereoselective reduction of prochiral ketones to the corresponding alcohols using biocatalysts has attracted much attention, from the viewpoint of green chemistry. Asymmetric reduction of indanone, tetralone and hydroxyl trimonoterpene ketones to the corresponding enantiomerically pure (S)-alcohols, using Daucus carota plant homogenate and fermented baker's yeast cells, is described. The present study illustrates the broad substrate selectivity of the dehydrogenase enzymes present in the D. carota in the synthesis of a wide range of chiral secondary alcohols of biological importance.