1438391-33-3

Basic information

• Product Name: 4-bromo-6-tert-butyldibenzo[b,d]furan
• Synonyms: 4-bromo-6-tert-butyldibenzo[b,d]furan;4-Bromo-6-(1,1-dimethylethyl)dibenzofuran;4-bromo-6-tert-butyldibenzo]furan
• CAS NO: 1438391-33-3
• Molecular Formula: C16H15BrO
• Molecular Weight: 303.1937
• Mol File: 1438391-33-3.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 381.1±22.0 °C(Predicted)
• Appearance: /
• Density: 1.357±0.06 g/cm3(Predicted)
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 4-bromo-6-tert-butyldibenzo[b,d]furan(CAS DataBase Reference)
• NIST Chemistry Reference: 4-bromo-6-tert-butyldibenzo[b,d]furan(1438391-33-3)
• EPA Substance Registry System: 4-bromo-6-tert-butyldibenzo[b,d]furan(1438391-33-3)

Safety Data

• Hazardous Substances Data: 1438391-33-3(Hazardous Substances Data)

Usage

General Description

4-bromo-6-tert-butyldibenzo[b,d]furan, also known as 2,2-dimethyl-3-(4-bromophenyl)dibenzo[b,d]furan, is a chemical compound with the molecular formula C22H19BrO. It is a dibenzofuran derivative with a bromine atom and a tert-butyl group attached to the benzene rings. 4-bromo-6-tert-butyldibenzo[b,d]furan is used in organic synthesis and has potential applications in the pharmaceutical and agrochemical industries. Its specific properties and uses are still being researched, but it is known to be a versatile building block for creating complex organic molecules with potential biological activity. Additionally, its unique structural features make it a valuable tool for scientists studying heterocyclic compounds and their potential applications.

Upstream product

• 507-19-7 t-butyl bromide 
• 201138-91-2 4,6-dibromodibenzo-[b,d]furan 

Relevant articles and documents

ORGANIC ELECTROLUMINESCENT COMPOUND AND ORGANIC ELECTROLUMINESCENT DEVICE

The present invention provides an organic electroluminescent compound and an organic electroluminescent device using the organic electroluminescent compound, the compound has the following structural formula: wherein R1, R2 and R4 are, each independently, selected from a group consisting of a hydrogen atom, a C1-C20 linear or branched alkyl group, a substituted or unsubstituted N-(phenylmethyl)imino group, a phenyl group, phenylamine, diphenylamine, phenyl pyridinylamine, bipyridinylamine, phenyl naphthylamine, binaphthylamine, phenyl phenanthrylamine, biphenanthrylamine, phenyl anthrylamine, bianthrylamine, phenanthridine, biphenyl, a pyridyl group, a pyrimidinyl group, a quinolinyl group and a triazinyl group; R3 is selected from a group consisting of hydrogen atom, a C1-C10 linear or branched alkyl group, a substituted or unsubstituted N-(phenylmethyl)imino group, a phenyl group, phenylamine, diphenylamine, phenyl pyridinylamine, bipyridinylamine, phenyl naphthylamine, binaphthylamine, phenyl phenanthrylamine, biphenanthrylamine, phenyl anthrylamine, bianthrylamine, phenanthridine, biphenyl, a pyridyl group, a pyrimidinyl group, a quinolinyl group and a triazinyl group.