140669-67-6

Upstream product

• 140669-71-2 (2-Amino-phenyl)-methyl-diphenyl-phosphonium; iodide 
• 615-36-1 2-bromoaniline 
• 603-35-0 triphenylphosphine 
• 95-51-2 o-chloroaniline 
• 140669-74-5 (2-Aminophenyl)(benzyl)diphenylphosphonium Bromide 
• 140669-72-3 (2-Amino-phenyl)-benzyl-diphenyl-phosphonium; chloride 
• 124843-09-0 (2-aminophenyl)triphenylphosphonium chloride 
• 140669-73-4 (2-Amino-phenyl)-triphenyl-phosphonium; bromide 
• 65423-44-1 (2-diphenylphosphino)benzeneamine 
• 67405-21-4 (+/-)-(2-Aminophenyl)phenylphosphine 
• 74-88-4 methyl iodide 

Downstream Products

• 160952-03-4 (R*,R*/S*)-1,3-Bis<<2-(methylphenylphosphino)phenyl>amino>propane 
• 160952-08-9 (+/-)[SP-4-2]-[(2-aminophenyl)methylphenylphosphine-N,P]dichloropalladium(II) 
• 160951-95-1 (+/-)[SP-4-2]-[(2-aminophenyl)methylphenylphosphine-N,P]dichloroplatinum(II) 
• 199343-32-3 [SP-4-2]-bis[(+/-)-(2-aminophenyl)methylphenylphosphine-P]dimethylplatinum(II) 
• 199296-93-0 [SP-4-2]-[(+/-)-(2-aminophenyl)methylphenylphosphine-P]chloro(methyl)platinum(II) 
• 199297-04-6 [SP-4-3]-[(2-aminophenyl)methylphenylphosphine-P][2-(methylphenylphosphine)phenylamido-N,P]methylplatinum(II) 
• 199296-96-3 [SP-4-2]-[(+/-)-(2-aminophenyl)methylphenylphosphine-P]oxalatoplatinum(II) 
• 198565-42-3 (T-4)-tris[(+/-)(2-aminophenyl)methylphenylphosphine]copper(I) hexafluorophosphate 
• 198565-40-1 (T-4)-bis[(+/-)-(2-aminophenyl)methylphenylphosphine]copper(I) hexafluorophosphate 
• 198565-17-2 (L-2)-bis[(+/-)-(2-aminophenyl)methylphenylphosphine]gold(I) iodide 
• 198565-11-6 (L-2)-[(+/-)-(2-aminophenyl)methylphenylphosphine]iodogold(I) 
• 195989-84-5 (+/-)-(2-aminophenyl)(2-chlorophenyl)methylphosphine 
• 31238-62-7 2-methylphosphanyl-aniline 

Relevant academic research and scientific papers

Synthesis, Resolution and Reactions of (+/-)-(2-Aminophenyl)methylphenylphosphine. Crystal and Molecular Structure of (R*,R*,S*,R*)-(+/-)-(1,3-Bisamino>propane)nickel(II) Perchlorate

Asymmetric bidentate (+/-)-(2-aminophenyl)methylphenylphosphine has been prepared in 80percent yield from (2-aminophenyl) diphenylphosphine via the secondary phosphine (+/-)-(2-aminophenyl)phenylphosphine.The chiral tertiary phosphine has been resolved by

Completely Stereoselective Synthesis of a Chiral Quadridentate Ligand with As2NP Donor Atoms. Crystal and Molecular Structure of *,S*)>-(+/-)-Dichloro--2-<(2-aminophenyl)methylphosph

Reaction of (+/-)-(2-aminophenyl)(2-chlorophenyl)methylphosphine with sodium (2-dimethylarsinophenyl)methylarsenide is completely stereoselective giving (R*,S*)-1--2-(2-aminophenyl)methylphosphi

Preparation of Hybrid Bidentate Phosphine Ligands by Reduction of Their Benzyl- or Phenyl-phosphonium Salts. X-Ray Crystal Structure of 2-Aminophenyltriphenylphosphonium Tetrachloronickelate(II)

The 2-substituted phenylphosphine bidentate hybrid ligands, 2-aminophenyl-, 2-methylaminophenyl-, 2-hydroxyphenyl- and (2-amino-3-methylphenyl)-diphenylphosphine, (1a-d), respectively, and 2-aminophenylmethylphenylphosphine, (1e), were synthesized by reduction of their phenylphosphonium halides, (2a-e)X (X = Cl or Br), with sodium naphthalenide in tetrahydrofuran at -68 deg, or electrochemically at a mercury cathode.The phosphonium salts were prepared by reaction of triphenylphosphine with aryl halide and anhydrous nickel halide at 200 deg.X-Ray diffraction of (2a)2 showed it to have monoclinic space group P21/n, a 10.657(4), b 20.966(3), c 20.422(6) Angstroem, β 101.33(2) deg and Z 4.The structure was refined by a full-matrix least-squares procedure to a final R 0.050 for 3534 reflections with I > 2.5?(I).