42501-87-1

Basic information

• Product Name: Benzenamine, N-[(2-fluorophenyl)methylene]-4-methoxy-
• CAS NO: 42501-87-1
• Molecular Formula: C14H12FNO
• Molecular Weight: 229.254
• Mol File: 42501-87-1.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: Benzenamine, N-[(2-fluorophenyl)methylene]-4-methoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, N-[(2-fluorophenyl)methylene]-4-methoxy-(42501-87-1)
• EPA Substance Registry System: Benzenamine, N-[(2-fluorophenyl)methylene]-4-methoxy-(42501-87-1)

Safety Data

• Hazardous Substances Data: 42501-87-1(Hazardous Substances Data)

Upstream product

• 104-94-9 4-methoxy-aniline 
• 89-99-6 2-fluorobenzylamine 
• 446-52-6 2-Fluorobenzaldehyde 

Downstream Products

• 1384176-02-6 ((2S,3S)-2-(2-fluorophenyl)-1-(4-methoxyphenyl)pyrrolidin-3-yl)methanol 
• 1440008-56-9 ((2S,3S)-2-(2-fluorophenyl)-1-(4-methoxyphenyl)piperidin-3-yl)methanol 
• 3295-60-1 2-methoxyacridine 
• 1512859-13-0 C₂₁H₂₀N₂O₂ 
• 1381866-30-3 4-(2-(2-fluorophenyl)-6-methoxy-3-methyl-1,2,3,4-tetrahydroquinolin-4-yl)-2-methoxyphenol 
• 1133378-62-7 (2S,3S)-2-(2-fluorophenyl)-1-(4-methoxyphenyl)-1,2,3,4-tetrahydropyridine-3-carbaldehyde 

Relevant articles and documents

Synthesis, structures, photoluminescent and electroluminescent properties of boron complexes with anilido-imine ligands

Syntheses of three new N-arylanilido-arylimine bidentate Schiff base type ligand precursors, ortho-C6H4[NH(2,6-iPr2C6H3)](CH{double bond, long}NAr1) [Ar1 = p-FC6

Paclitaxel Biosynthesis: Adenylation and Thiolation Domains of an NRPS TycA PheAT Module Produce Various Arylisoserine CoA Thioesters

Structure-activity relationship studies show that the phenylisoserinyl moiety of paclitaxel (Taxol) is largely necessary for the effective anticancer activity. Several paclitaxel analogues with a variant isoserinyl side chain have improved pharmaceutical

Ir-Catalyzed C?H Amidation of Aldehydes with Stoichiometric/Catalytic Directing Group

Ir-catalyzed sp2C?H amidation of aldehydes with various anilines as stoichiometric or catalytic directing groups was accomplished. A wide range of substrates were selectively amidated in good to excellent yields with broad functional group tolerance. The iridacycle complexes were isolated, characterized, and proved as key intermediates. Kinetic studies and Hammett plots provided detailed understandings of this amidation. According to the mechanism, the electron-rich ArSO2N3was proved effective for intermolecular sp3C?H amidation.