26508-67-8

Basic information

• Product Name: tri-p-tolylantimony dichloride
• Synonyms: tri-p-tolylantimony dichloride
• CAS NO: 26508-67-8
• Molecular Weight: 466.054
• Mol File: 26508-67-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: tri-p-tolylantimony dichloride(CAS DataBase Reference)
• NIST Chemistry Reference: tri-p-tolylantimony dichloride(26508-67-8)
• EPA Substance Registry System: tri-p-tolylantimony dichloride(26508-67-8)

Safety Data

• Hazardous Substances Data: 26508-67-8(Hazardous Substances Data)

Upstream product

• 5395-43-7 tri(p-tolyl)antimony 
• 78989-73-8 (CH₃(C₆H₄))3Sb(ONC(CH₂)5)2 
• 10026-07-0 tellurium tetrachloride 
• 7440-36-0 antimony 
• 10025-91-9 antimony(III) chloride 
• 141-78-6 ethyl acetate 
• 4294-57-9 para-methylphenylmagnesium bromide 
• 106-38-7 para-bromotoluene 
• 81952-61-6 N-tri-p-tolylantimony bis(triphenylphosphinimine) 
• 484674-58-0 O-tri(p-methylphenyl)antimony(V) di(methylphenyloximate) 
• 29510-67-6 phenyltellurium(IV) trichloride 

Downstream Products

• 129180-31-0 (CH₃C₆H₄)3Sb{(C₆H₄(O)CHN)2C₆H₄} 
• 64634-43-1 (4-CH₃C₆H₄)2SbC₆H₄-4-F 
• 121974-85-4 (4-CH₃C₆H₄)2SbCCSb(4-CH₃C₆H₄) 
• 130681-43-5 (CH₃C₆H₃O)2NHSb(CH₃C₆H₄)3 
• 130681-42-4 {(C(CH₃)3)2C₆H₂O}2NHSb(CH₃C₆H₄)3 
• 130681-30-0 C₁₂H₆NO₂Sb(CH₃)2(C₆H₄CH₃)2 
• 106-43-4 para-chlorotoluene 
• 87856-04-0 chlorobis(4-methylphenyl)antimony 

Relevant articles and documents

121Sb Moessbauer and 1H and 13C NMR Spectroscopic Studies of a Series of Organoantimony(V) Compounds, R3SbX2

The 121Sb Moessbauer spectroscopic and the 1H and 13C NMR nuclear magnetic resonance studies have been performed for a series of organoantimony(V) compounds: R3SbX2 (R=CH3, C6H5, p-CH3C6H4; X=F, Cl, Br, I).For the trimethylantimony dihalides, the isomer shifts and quadrupole coupling constants of the 121Sb Moessbauer spectra indicated that the withdrawal of the bonding electrons from the antimony atom along Sb-X increased, as the electronegativity of the halogen increased.The chemical shifts of the 1H and 13C NMR spectra showed that the electron population around the methyl group increased with increasing electronegativity of halogen.For phenyl and p-tolyl derivatives, both 121Sb Moessbauer and 13C NMR data showed a trend similar to the methyl compounds.The results suggest that the electron cloud around the antimony atom spreads, with an increase in the electronegativity of the halogen, not only toward the halogen atoms but also toward the plane perpendicular to the bonding direction with the halogen atoms.