1382763-45-2

Upstream product

• 1993-03-9 o-fluorophenylboronic acid 
• 3401-47-6 1-bromo-2-methoxynaphthalene 
• 573-97-7 1-bromo-2-naphthol 
• 1023674-80-7 9-(3-bromophenyl)-10-phenylanthracene 
• 1382763-54-3 (benzo[b]naphtho[1,2-d]furan-6-yl)boronic acid 
• 205-39-0 benzo[b]naphtho[1,2-d]furan 
• 1264712-17-5 1-(2-fluorophenyl)naphthalen-2-ol 
• 1382763-56-5 1-(2-fluorophenyl)-2-methoxynaphthalene 

Relevant academic research and scientific papers

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.

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.