1382763-56-5

Basic information

• Product Name: 1-(2-fluorophenyl)-2-methoxynaphthalene
• Synonyms: 1-(2-fluorophenyl)-2-methoxynaphthalene
• CAS NO: 1382763-56-5
• Molecular Weight: 252.288
• Mol File: 1382763-56-5.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 1-(2-fluorophenyl)-2-methoxynaphthalene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2-fluorophenyl)-2-methoxynaphthalene(1382763-56-5)
• EPA Substance Registry System: 1-(2-fluorophenyl)-2-methoxynaphthalene(1382763-56-5)

Safety Data

• Hazardous Substances Data: 1382763-56-5(Hazardous Substances Data)

Upstream product

• 3401-47-6 1-bromo-2-methoxynaphthalene 
• 1993-03-9 o-fluorophenylboronic acid 

Downstream Products

• 1264712-17-5 1-(2-fluorophenyl)naphthalen-2-ol 
• 1383607-08-6 6-phenylbenzo[b]naphtho[1,2-d]furan 
• 1382763-43-0 6-[3-(9,10-diphenyl-2-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 
• 1382763-49-6 6-[4-(10-phenyl-9-anthryl)phenyl]-benzo[b]naphtho[1,2-d]furan 
• 205-39-0 benzo[b]naphtho[1,2-d]furan 
• 1382763-45-2 6-[3-(10-phenyl-9-anthryl)phenyl]-benzo[b]naphtho[1,2-d]furan 

Relevant articles and documents

Synthesis of a class of binaphthyl monophosphine ligands with a naphthofuran skeleton and their applications in Suzuki-Miyaura coupling reactions

A series of new monophosphine ligands containing a naphthofuran skeleton have been prepared, characterized and evaluated in palladium-catalyzed Suzuki-Miyaura coupling reactions. Using Pd2(dba)3-L6 as the catalyst the reactions were performed with high catalytic activity under mild reaction conditions and the desired coupling products were obtained in good to excellent yields. The new catalyst system also showed broad substrate adaptability and practicality for gram-scale production.

Anionic phospho-fries rearrangement at ferrocene: One-pot approach to P,O-substituted ferrocenes

For the first time the anionic phospho-Fries rearrangement has been successfully applied in ferrocene chemistry, giving access to 1,2-P,O-substituted ferrocenes. The 1,3 (O → C)-migration occurs at ferrocenyl phosphates, thiophosphates, phosphite-borane adducts, and phosphinates by treatment with a base such as lithium diisopropylamide at low temperature, whereas the highest yields were obtained starting from diethylferrocenyl phosphate. Complete reduction of the phosphonate to a primary phosphine and subsequent Stelzer P,C cross coupling allowed the synthesis of Fe(η5-C5H3-2-OMe-PPh2) (η5-C5H5) (1). The qualification of 1 as a supporting ligand in palladium-catalyzed Suzuki-Miyaura C,C couplings has been proven by the synthesis of sterically congested tri-ortho-substituted biaryls under mild reaction conditions in good to excellent yields.

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.