960079-28-1

Basic information

• Product Name: 4-BroMo-1,1,3,3,5,5,7,7-octaethyl-1,2,3,5,6,7-hexahydro-s-indacene
• Synonyms: 4-BroMo-1,1,3,3,5,5,7,7-octaethyl-1,2,3,5,6,7-hexahydro-s-indacene;4-Bromo-1,1,3,3,5,5,7,7-octaethyl-1,2,3,5,6,7-hexahydro-s-indacene
• CAS NO: 960079-28-1
• Molecular Formula: C₂₈H₄₅Br
• Molecular Weight: 461.5609
• Mol File: 960079-28-1.mol
• Article Data: 2

Chemical Properties

• Melting Point: 153.0 to 157.0 °C
• Boiling Point: 463.6±45.0 °C(Predicted)
• Appearance: /
• Density: 1.007±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 4-BroMo-1,1,3,3,5,5,7,7-octaethyl-1,2,3,5,6,7-hexahydro-s-indacene(CAS DataBase Reference)
• NIST Chemistry Reference: 4-BroMo-1,1,3,3,5,5,7,7-octaethyl-1,2,3,5,6,7-hexahydro-s-indacene(960079-28-1)
• EPA Substance Registry System: 4-BroMo-1,1,3,3,5,5,7,7-octaethyl-1,2,3,5,6,7-hexahydro-s-indacene(960079-28-1)

Safety Data

• Hazardous Substances Data: 960079-28-1(Hazardous Substances Data)

Usage

Uses

Used in Organic Electronics:
4-bromo-1,1,3,3,5,5,7,7-octaethyl-1,2,3,5,6,7-hexahydro-s-indacene is used as a component in organic electronics for its unique photophysical properties that can enhance the performance of electronic devices.
Used in Photovoltaics:
In the photovoltaic industry, 4-bromo-1,1,3,3,5,5,7,7-octaethyl-1,2,3,5,6,7-hexahydro-s-indacene is utilized for its potential to improve the efficiency of solar cells by leveraging its light-absorbing characteristics.
Used in Organic Synthesis:
4-bromo-1,1,3,3,5,5,7,7-octaethyl-1,2,3,5,6,7-hexahydro-s-indacene serves as a valuable intermediate in organic synthesis, particularly due to the reactivity of the bromine atom, which can be substituted in various chemical reactions to produce a range of derivative compounds.
Used in Medicinal Chemistry:
In medicinal chemistry, 4-bromo-1,1,3,3,5,5,7,7-octaethyl-1,2,3,5,6,7-hexahydro-s-indacene is used as a building block for the development of new pharmaceuticals, taking advantage of its structural features to design molecules with specific biological activities.

Upstream product

• 1459-93-4 dimethyl Isophthalate 
• 960079-26-9 1,3-bis(1-chloro-1-ethylpropyl)benzene 
• 676465-94-4 1,3-bis(1-ethyl-1-hydroxypropyl)benzene 
• 960079-27-0 1,1,3,3,5,5,7,7-octaethyl-s-hydrindacene 

Downstream Products

• 1620487-87-7 (E)-1,2-bis(1-naphthyl)-1,2-bis(1,1,3,3,5,5,7,7-octaethyl-shydrindacen-4-yl)disilene 
• 960079-31-6 (1,1,3,3,5,5,7,7-octaethyl-s-hydrindacene-4-yl)phenylsilane 
• 1187583-29-4 (E)-1,2-bis(1,1,3,3,5,5,7,7-octaethyl-s-hydrindacen-4-yl)-2-phenylphosphasilene 
• 960079-24-7 dibromo(1,1,3,3,5,5,7,7-octaethyl-s-hydrindacene-4-yl)phenylsilane 

Relevant articles and documents

Synthesis and Structures of a Series of Bulky "Rind-Br" Based on a Rigid Fused-Ring s-Hydrindacene Skeleton

A series of octa-R-substituted bromo-s-hydrindacenes, "Rind-Br," have been synthesized by a sequence of the Lewis acid catalyzed intramolecular FriedelCrafts reaction, bromination and vice versa. Their structural features and physical properties depend on

Coplanar oligo(p-phenylenedisilenylene)s based on the octaethyl-substituted s-hydrindacenyl groups

The silicon analogues of the oligo(p-phenylenevinylene)s (Si-OPVs) with highly planar structures have been synthesized using a newly developed ligand, the 1,1,3,3,5,5,7,7-octaethyl-s-hydrindacen-4-yl (Eind) group. Their X-ray crystal structures and spectr