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

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

Uses

Used in Chemical Research:
2H-INDEN-2-ONE, 5-BROMO-1,3-DIHYDROis utilized as a research chemical for the study of its unique properties and potential applications in various scientific fields. Its brominated structure and cyclic ketone group make it a valuable subject for investigations into chemical reactions and synthesis processes.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2H-INDEN-2-ONE, 5-BROMO-1,3-DIHYDROmay serve as an intermediate or a building block in the synthesis of new drugs or drug candidates. Its specific chemical features could contribute to the development of novel therapeutic agents with unique mechanisms of action.
Used in Material Science:
2H-INDEN-2-ONE, 5-BROMO-1,3-DIHYDROcould be employed in material science for the development of new materials with specific properties. Its chemical structure may influence the physical and chemical characteristics of materials, such as stability, reactivity, or conductivity.
Used in Environmental Applications:
2H-INDEN-2-ONE, 5-BROMO-1,3-DIHYDROmay also find use in environmental applications, such as in the development of methods for the detection or remediation of pollutants. Its chemical properties could be leveraged to create new tools for environmental monitoring and protection.

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

Upstream product

• 862135-60-2 5-bromoindan-2-ol acetate 
• 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 
• 4254-31-3 2-acetoxyindane 

Downstream Products

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

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.

LIQUID CRYSTAL COMPOUND, LIQUID CRYSTAL COMPOSITION, AND LIQUID CRYSTAL DISPLAY DEVICE

PROBLEM TO BE SOLVED: To provide a liquid crystal compound, a liquid crystal composition, and a liquid crystal device using the compound or the composition. SOLUTION: The liquid crystal compound is represented by formula (I). In formula (I), R1 represents H, an alkyl having 1 to 10 carbon atoms, or the like; R2 represents an alkenyl having 2 to 10 carbon atoms or a fluoroalkenyl having 2 to 10 carbon atoms and one or two non-adjacent -CH2- in R2 is replaced by -O- or an ether having 2 to 10 carbon atoms; A1 to A4 each independently represent a formula below, where R3 independently represents H or a halogen; Z1 to Z3 each independently represents a sing bond, -CH2-, -CH2O-, -OCH2-, -CF=CF-, -COO-, -OCO-, -CF2O-, -OCF2-, -C≡C-, -CH=CH-, or the like; and n and m each independently represent 0 or 1. SELECTED DRAWING: None COPYRIGHT: (C)2016,JPOandINPIT

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.