1382763-54-3

Usage

Uses

Used in Organic Chemistry:
(Benzo[b]naphtho[1,2-d]furan-6-yl)boronic acid is utilized as a reagent in organic chemistry, particularly for the synthesis of various pharmaceutical and biologically active molecules. Its boronic acid group allows for a range of reactions, making it a versatile building block in the creation of complex organic compounds.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (benzo[b]naphtho[1,2-d]furan-6-yl)boronic acid serves as an intermediate in the development of new drugs and therapeutic agents. (benzo[b]naphtho[1,2-d]furan-6-yl)boronic acid's unique structure and biological activities contribute to its potential as a promising candidate for pharmaceutical applications.
Used in Materials Science:
The potential application of (benzo[b]naphtho[1,2-d]furan-6-yl)boronic acid in materials science stems from its unique structure and properties. Researchers are exploring its use in the development of novel materials with specific characteristics, such as improved mechanical strength or enhanced chemical reactivity.
Used in Catalysis:
(Benzo[b]naphtho[1,2-d]furan-6-yl)boronic acid's unique structure also makes it a candidate for use in catalysis, where it could potentially facilitate or enhance various chemical reactions. Its application in this field is currently a subject of ongoing research and exploration.

Upstream product

• 205-39-0 benzo[b]naphtho[1,2-d]furan 
• 121-43-7 Trimethyl borate 

Downstream Products

• 1382763-45-2 6-[3-(10-phenyl-9-anthryl)phenyl]-benzo[b]naphtho[1,2-d]furan 
• 1382763-47-4 6-[4-(9,10-diphenyl-2-anthryl)phenyl]-benzo[b]naphtho[1,2-d]furan 
• 1382763-43-0 6-[3-(9,10-diphenyl-2-anthryl)phenyl]-benzo[b]naphtho[1,2-d]furan 
• 1383607-08-6 6-phenylbenzo[b]naphtho[1,2-d]furan 

Relevant academic research and scientific papers

Novel hole transport materials based on triarylamine/naphtho[2,1-b]benzofunan for efficient green electroluminescent device

Two hole transport materials, N-([1,1'-biphenyl]-4-yl)-9,9-dimethyl-N-(4-(naphtho[2,1-b]benzofuran-6-yl)phenyl)-9H-fluoren-2-amine (DFA) and N-(9,9-dimethyl-9H-fluoren-2-yl)-9,9-dimethyl-7-(naphtho[2,1-b]benzofuran-6-yl)-N-phenyl-9H-fluoren-2-amine (TFA) were designed, synthesized and fully characterized. The photophysical and thermal properties of these two compounds were investigated by UV–vis absorption spectra, photoluminescence spectra, thermogravimetric analysis (TGA) and differential scanning calorimetry analysis (DSC), which indicated that DFA and TFA would be efficient hole transport materials due to their proper HOMO energy levels and excellent thermal stability. Then, green OLEDs with DFA and TFA as hole transport layer, respectively, were fabricated, NPB-based OLEDs was also prepared for comparison. It turned out that DFA- and TFA-based devices exhibited higher efficiencies than that of NPB-based device, and TFA-based device showed the best performances with current efficiency, power efficiency and external quantum efficiency of 41.68 cd/A, 32.04 lm/W and 12.04%, respectively.

Benzo[b]Naphtho[1,2-d]Furan Compound as Light-Emitting Element Material

Provided is a benzo[b]naphtho[1,2-d]furan compound having a wide band gap which gives excellent color purity of blue. Further provided are a light-emitting element, a light-emitting device, and an electronic device each of which uses the benzo[b]naphtho[1,2-d]furan compound and is highly reliable. A benzo[b]naphtho[1,2-d]furan compound represented by a general formula (G1) is provided. In the general formula (G1), An represents an anthryl group represented by a general formula (An-1) or (An-2) below, α1 and α2 separately represent a substituted or unsubstituted phenylene group represented by any one of general formulae (α-1) to (α-3) below, and R1 to R9 separately represent either hydrogen or an alkyl group having 1 to 4 carbon atoms. Further, in the general formula (G1), n and m separately represent 0 or 1.

Organoboron Compound and Method for Manufacturing the Same

To provide a novel organoboron compound which is useful as a reactant of organic synthesis. To provide a method for manufacturing the organoboron compound. A novel organoboron compound represented by General Formula (G1) below is provided. Note that in General Formula (G1), R1 to R9 separately represent any one of hydrogen, an alkyl group having 1 to 6 carbon atoms, and an aryl group having 6 to 16 carbon atoms. R10 and R11 separately represent hydrogen or an alkyl group having 1 to 6 carbon atoms, and R10 and R11 may be bonded with each other to form a ring. Further, X represents an oxygen atom or a sulfur atom.