30895-98-8

Basic information

• Product Name: 4-methylphenyltellurium trichloride
• Synonyms: 4-methylphenyltellurium trichloride
• CAS NO: 30895-98-8
• Molecular Weight: 325.092
• Mol File: 30895-98-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 4-methylphenyltellurium trichloride(CAS DataBase Reference)
• NIST Chemistry Reference: 4-methylphenyltellurium trichloride(30895-98-8)
• EPA Substance Registry System: 4-methylphenyltellurium trichloride(30895-98-8)

Safety Data

• Hazardous Substances Data: 30895-98-8(Hazardous Substances Data)

Upstream product

• 17841-80-4 bis(tri-p-tolyltin) oxide 
• 108-88-3 toluene 
• 3728-43-6 p-(trimethylsilyl)toluene 
• 539-43-5 4-methylphenylmercuric chloride 

Downstream Products

• 79313-60-3 bis(p-tolyltellanyl)selane 
• 1246345-89-0 C₁₃H₁₃Cl₂NTe 
• 1204704-30-2 C₃₁H₂₃Cl₂NTe 
• 172166-51-7 trimethylsilylmethylbis(p-tolyltelluro)antimony 
• 644-08-6 4-Methylbiphenyl 
• 56950-02-8 n-butyl 4-methylphenyl telluride 
• 837-13-8 di(p-methylphenyl)tellurium dichloride 
• 624-31-7 4-tolyl iodide 
• 106-43-4 para-chlorotoluene 
• 95-73-8 2,4-dichlorotoluene 
• 613-33-2 (4,4'-dimethyl-1,1'-biphenyl) 
• 115022-74-7 C₁₂H₁₆Cl₂OTe 
• 32294-57-8 bis(4-methylphenyl)ditelluride 

Relevant articles and documents

On the reactivity of metal and organometallic halides toward r 3sn-o-snr3 systems

Interaction of metallic salts (M = Hg, Sb, and Te) with bis(triorganotin) oxide, (R3Sn)2O, where (R = C6H5, p-CH3C6H4, and cyclo-C6H 11) at room temperature

Chalcogeno-Substituted Bis-triphenylmethylium Ions of the Inverse Malachite Green Type

The longest wavelength VIS absorptions of the deeply colored CF3CO2H solutions of the 4,4'-chalcogenobis-(triphenylmethylium) ions 4(++), Y2 (Y = O, S, Se, Te) resemble closely those of the corresponding monocationic 4-arylchalcogenotriphenylmethylium systems 5(1+), ArYC6H4C(1+)(C6H5)2, and not those of the structurally directly related 4,4'-bis(arylchalcogeno)triphenylmethylium ions 3(1+), C6H5C(1+)(C6H4YAr)2.This is in striking contrast to the results obtained previously for analogous nitrogen systems, where "inverse", 2(++), RN, and "conventional" malachite green systems 1(+), (Ar2NC6H4)2C(1+)R, yield almost identical λmax values.A rationalization of these observations can be achieved based on the assumption of largely delocalized dications 2(++) versus more or less orthogonal "double monocationic" systems 4B(++), separated due to torsional twist.Whereas the formal push-pull systems 6(+), ArSC6H4YC6H4C(1+)(C6H5)2 (Y = O, S, Se) behaved practically like the corresponding standard systems 5(+), the mono- and bis-triphenylmethylthio-substituted dibenzofuran, dibenzothiophene and thioxanthene derivatives 8(+), 9(++), 10(+) and 11(++) displayed hypsochromic shifts of their color bands relative to their noncyclic analogues which are only partly in accordance with predictions based on a simple frontier orbital Hueckel model.The 1H and 13C NMR spectra of all these cationic species comply with their respective charges. +"--"+ Dyes, Chalcogeno-bis-trityliumions, VIS Spectra, NMR Spectra