174702-59-1

Basic information

• Product Name: 4-Bromo-2-methyl-1-indanone
• Synonyms: 4-Bromo-2-methyl-1-indanone;4-broMo-2-Methyl-2,3-dihydro-1H-inden-1-one;4-bromo-2-methyl-2,3-dihydroinden-1-one;1H-Inden-1-one,4-bromo-2,3-dihydro-2-methyl-
• CAS NO: 174702-59-1
• Molecular Formula: C₁₀H₉BrO
• Molecular Weight: 225
• EINECS: 1533716-785-6
• Mol File: 174702-59-1.mol
• Article Data: 6

Chemical Properties

• Melting Point: 27 °C
• Boiling Point: 131-134℃ (2 Torr)
• Flash Point: 99.4±12.2℃
• Appearance: /
• Density: 1.488±0.06 g/cm3 (20℃ 760 Torr)
• Storage Temp.: Sealed in dry,Room Temperature
• Solubility: soluble in Toluene
• CAS DataBase Reference: 4-Bromo-2-methyl-1-indanone(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Bromo-2-methyl-1-indanone(174702-59-1)
• EPA Substance Registry System: 4-Bromo-2-methyl-1-indanone(174702-59-1)

Safety Data

• Hazardous Substances Data: 174702-59-1(Hazardous Substances Data)

Usage

General Description

4-Bromo-2-methyl-1-indanone is a chemical compound with the molecular formula C10H9BrO. Its systematic name is 1-bromo-2-methyl-3H-inden-1-one. Possessing a molar mass of approximately 227.08 g/mol, it appears as a white or off-white solid. It falls under the category of organobromides and ketones. Information on its physical properties such as boiling point, melting point, or density is limited, possibly due to its less common nature or specialized use in chemistry. As with many bromine-containing organic compounds, it should be handled with care due to potential reactivity and toxicity issues. Specific applications, health risks, and environmental impacts of this chemical compound are not well documented. It's often used in laboratory settings for specific syntheses or reactions.

Upstream product

• 6630-33-7 ortho-bromobenzaldehyde 
• 1311148-31-8 (E)-3-(2-bromophenyl)-2-methylacrylaldehyde 
• 869063-66-1 3-(2-bromophenyl)-2-methylpropionyl chloride 
• 19829-31-3 1-(3-bromophenyl)-1-propanone 

Downstream Products

• 880652-93-7 4⁽⁷⁾-bromo-2-methyl-1⁽³⁾H-indene 

Relevant articles and documents

Process for the Preparation of Idnanones

A process of forming compounds of formula I comprising the steps of addition of an amino compound H2NR to a compound of formula (II) followed by cyclization, isomerization and hydrolysis.

HALOGEN SUBSTITUTED METALLOCENE COMPOUNDS FOR OLEFIN POLYMERIZATION

A metallocene compound is represented by the formula (1): AMXn-1 wherein M is a transition metal atom having a coordination number of n selected from Group 3, 4, 5 or 6 of the Periodic Table of Elements, or a lanthanide metal atom, or actinide metal atom; A is a substituted monocyclic or polycyclic arenyl ligand pi-bonded to M, wherein said arenyl ligand includes at least one halogen substituent directly bonded to any sp2 carbon atom at a bondable ring position of the ligand; and the or each X is a univalent anionic ligand, or two X are joined and bound to the metal atom to form a metallocycle ring, or two X are joined to form a chelating ligand, a diene ligand, or an alkylidene ligand.

Preparation of preparing substituted indanones

a process for the preparation of indanones of the formula II from, indanones of the formula I or of indanones of the formula IIa from indanones of the formula Ia comprises reacting an indanone of the formula I or Ia with a coupling component.