797056-48-5

Usage

Uses

Used in Synthetic Organic Chemistry:
2'-Bromospiro[cyclohexane-1,9'-fluorene] is used as a building block for the synthesis of complex molecules, leveraging its high reactivity to facilitate various chemical reactions. This application is crucial for creating new compounds with potential applications across different industries.
Used in Materials Science:
In the field of materials science, 2'-Bromospiro[cyclohexane-1,9'-fluorene] is utilized for its unique physical and chemical properties, which can contribute to the development of advanced materials with specific characteristics required for various applications.
Used in Organic Electronics:
2'-broMospiro[cyclohexane-1,9'-fluorene]'s spirocyclic structure and reactivity make it a valuable component in organic electronics, where it can be employed in the design and synthesis of novel electronic materials and devices, potentially improving their performance and functionality.
Used in Pharmaceutical Development:
2'-Bromospiro[cyclohexane-1,9'-fluorene] is also used in the pharmaceutical industry as a precursor in the synthesis of new drugs, taking advantage of its reactive nature to create molecules with potential therapeutic effects.

Upstream product

• 7258-61-9 spiro 
• 111-24-0 1,5-dibromo-pentane 
• 1133-80-8 2-bromo-9H-fluorene 

Downstream Products

• 885684-39-9 C₃₆H₃₂N₂ 
• 885684-24-2 C₂₄H₂₃N 

Relevant academic research and scientific papers

Nitrogen-containing compound, organic electroluminescent element and electronic device

The invention belongs to the technical field of organic materials, and provides a nitrogen-containing compound, an organic electroluminescent device and an electronic device. The structure of the nitrogen-containing compound is represented by a chemical f

ORGANIC COMPOUND AND ORGANIC ELECTROLUMINESCENT DEVICE USING SAME

A novel compound having excellent light emission and heat stability is disclosed. Also disclosed is an organic electroluminescent device having properties such as light emitting efficiency, an operation voltage, and a service life improved by including th

An organic compound and an organic light emitting device comprising the same

The present invention relates to an organic compound having excellent chemical stability, charge mobility, and interfacial properties, and to an organic electroluminescent device including the same. The organic compound is represented by chemical formula

Compounds and organic electronic devices comprising the same

The present invention relates to compounds and organic electronic devices comprising the same. The compound of the present specification is used for an organic electronic device typified by an organic light emitting device, which can reduce the driving voltage of the organic electronic device, improve the light efficiency, and can improve the lifetime characteristics of the device by the thermal stability of the compound.

ARYLAMINE COMPOUND AND ORGANIC ELECTROLUMINESCENCE DEVICE CONTAINING THE SAME

Provided are a novel arylamine compound of a specific structure having at least one spiro bond; an organic EL device in which an organic compound layer comprising one layer or plural layers including at least a luminescent layer is interposed between a ca

AROMATIC AMINE DERIVATIVE AND ORGANIC ELECTROLUMINESCENT DEVICE USING SAME

Disclosed is a novel aromatic amine derivative having an asymmetric structure. Also disclosed is an organic electroluminescent device wherein an organic thin film composed of one or more layers including at least a light-emitting layer is interposed between a cathode and an anode. Since at least one layer of the organic thin film contains the aromatic amine derivative by itself or as a component of a mixture, molecules are hardly crystallized, thereby improving the production yield of the organic electroluminescent device. This organic electroluminescent device has a long life.

AROMATIC AMINE DERIVATIVE AND ORGANIC ELECTROLUMINESCENT DEVICE USING SAME

Disclosed is an organic electroluminescent device wherein an organic thin film which is composed of one or more layers including at least a light-emitting layer is interposed between a cathode and an anode. Since at least one layer of the organic thin film contains a novel aromatic amine derivative, which has an asymmetric structure wherein two different amine units are bonded through a linking group, by itself or as a component of a mixture, molecules are hardly crystallized, thereby improving the production yield of the organic electroluminescent device. This organic electroluminescent device has a long life.

AROMATIC AMINE COMPOUND AND ORGANIC ELECTROLUMINESCENT DEVICE USING SAME

Disclosed is an aromatic amine compound of a specific structure having at least one fluorene structure represented by the formula (1) below. Also disclosed is an organic electroluminescent device wherein an organic thin film composed of one or more layers including at least a light-emitting layer is interposed between a cathode and an anode and at least one layer in the organic thin film contains the aromatic amine compound by itself or as a component of a mixture. Such an organic electroluminescent device has various luminescent hues, high heat resistance, long life, high luminance and high luminous efficiency. The above-mentioned novel aromatic amine compound enables to realize such an organic electroluminescent device. (In the formula below, Ar1-Ar6 independently represent a substituted or unsubstituted aryl group having 5-60 nuclear carbon atoms or the like, and L1-L3 independently represent a substituted or unsubstituted arylene group having 5-60 nuclear carbon atoms or the like.)

ANTHRACENE DERIVATIVES AND ORGANIC ELECTROLUMINESCENT DEVICES MADE BY USING THE SAME

An anthracene derivative represented by the following general formula (1) which enables an organic electroluminescence device to exhibit a great efficiency of light emission and uniform light emission even at high temperatures since crystallization is suppressed and no thermal decomposition takes place during vapor deposition and an organic electroluminescence device utilizing the derivative, are provided. [Ar represents a group represented by the following general formula (2): (L1 and L2 each represent a substituted or unsubstituted methylene group, ethylene group or the like, and at least one of them is present), Ar' represents a substituted or unsubstituted aryl group having 6 to 50 nuclear carbon atoms, X represent an alkyl group or the like, a and b each represent an integer of 0 to 4, and n represents an integer of 1 to 3.]