2574-32-5

Upstream product

• 10025-91-9 antimony(III) chloride 
• 3910-39-2 tris(pentafluorophenyl)antimony 
• 830-48-8 dichloro(pentafluorophenyl)borane 
• 7783-56-4 antimony(III) fluoride 

Downstream Products

• 124782-52-1 (C₆F₅)2Sb(NCOCOC₆H₄) 
• 124782-51-0 (C₆F₅)2Sb(NCOCH₂CH₂CO) 
• 886577-55-5 (pentafluorophenyl)2(methyl)antimony(III) 
• 886577-56-6 (pentafluorophenyl)2(C₆H₄CH₃-p)antimony(III) 
• 7647-14-5 sodium chloride 
• 286401-34-1 bis(pentafluorophenyl)antimony(III) 2-methoxybenzoate 
• 21041-56-5 (pentafluorophenyl)2(phenyl)antimony(III) 

Relevant academic research and scientific papers

Synthesis and spectroscopic studies on some new pentafluorophenylantimony(III and V) derivatives

The oxidative addition reaction of (C6F5)2SbCl with ICl and IN3 yielded (C6F5)2SbI(X)Cl (X = Cl, N3). (C6F5)2SbN3 and (C6F5)2SbCl(NCS)N3 were synthesized by the displacement reactions of (C6F5)2SbCl with NaN3 in the presence of 15-crown-5 or (C6F5)2SbI(N3)Cl with AgNCS, respectively. The reaction of bis(pentafluorophenyl)antimony(V) azido derivatives with PhNCS yielded the corresponding 1,2-cycloaddition products i.e., tetrazole-5-thiones The compounds were characterised by elemental analyses, UV, IR and 19F NMR spectroscopic studies.

TRIORGANOANTIMONY COMPOUNDS FOR PESTICIDAL USE

The invention concerns with synthesis of mixed triorganoantimony (III) compounds bearing halophenyl groups ("R2SbR1") , using metal turnings viz Lithium, Magnesium or Zinc in donor solvents with plurality of uses as microbiocides and insecticides for cont