892575-08-5

Basic information

• Product Name: 4-Bromo-2-isopropyl-1-indanone
• Synonyms: 4-Bromo-2-isopropyl-1-indanone;2-isopropyl-4-broMo-1-indanone;4-Bromo-2,3-dihydro-2-(1-methylethyl)-1H-inden-1-one
• CAS NO: 892575-08-5
• Molecular Formula: C12H13BrO
• Molecular Weight: 253
• EINECS: 1533716-785-6
• Mol File: 892575-08-5.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-Bromo-2-isopropyl-1-indanone(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Bromo-2-isopropyl-1-indanone(892575-08-5)
• EPA Substance Registry System: 4-Bromo-2-isopropyl-1-indanone(892575-08-5)

Safety Data

• Hazardous Substances Data: 892575-08-5(Hazardous Substances Data)

Usage

General Description

4-Bromo-2-isopropyl-1-indanone is a specialized chemical compound with the molecular formula C12H13BrO. This substance is categorized under the classification of indanones, a subgroup of organic compounds known for having a distinct structural core made up of a fused cyclohexenone and benzene ring. It carries an isopropyl functional group on the second carbon and a bromine atom on the fourth carbon of the indanone backbone. This chemical's properties, such as its melting point, boiling point, and solubility, are dependent on factors like purity and temperature. It is typically used for research purposes and in various chemical reactions due to its unique reactivity.

Relevant articles and documents

HALOGEN SUBSTITUTED METALLOCENE COMPOUNDS FOR OLEFIN POLYMERIZATION

A metallocene compound is represented by the formula (1): wherein: M is a Group 3, 4, 5 or 6 transition metal atom, or a lanthanide metal atom, or actinide metal atom, preferably a Group 4 transition metal atom selected from titanium, zirconium or hafnium; E is a substituted or unsubstituted monocyclic or polycyclic arenyl ligand pi-bonded to M; A is a substituted or unsubstituted polycyclic arenyl ligand that is pi-bonded to M and has a different ring structure than the E ligand; at least one of the A and E ligands includes at least one halogen substituent directly bonded to an sp2 carbon at a bondable ring position; Y is a bridging group containing at least one Group 13, 14, 15, or 16 element and any single position of the ring structure of A and to any single position of the ring structure of E; and y is zero or 1, indicating the absence (y = 0) or presence (y =1) of Y; and 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; provided that when E is an unsubstituted cyclopentadienyl ligand, either y is one or A is not 2-bromofluorenyl or 2,7-dibromofluorenyl.

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.