4456-36-4

Basic information

• Product Name: di(p-methoxyphenyl)tellurium dichloride
• Synonyms: di(p-methoxyphenyl)tellurium dichloride
• CAS NO: 4456-36-4
• Molecular Weight: 412.77
• Mol File: 4456-36-4.mol
• Article Data: 15

Chemical Properties

• CAS DataBase Reference: di(p-methoxyphenyl)tellurium dichloride(CAS DataBase Reference)
• NIST Chemistry Reference: di(p-methoxyphenyl)tellurium dichloride(4456-36-4)
• EPA Substance Registry System: di(p-methoxyphenyl)tellurium dichloride(4456-36-4)

Safety Data

• Hazardous Substances Data: 4456-36-4(Hazardous Substances Data)

Upstream product

• 4456-34-2 bis(4-methoxyphenyl)telluride 
• 100-66-3 methoxybenzene 
• 4346-59-2 para-methoxyphenyldiazonium chloride 
• 61948-97-8 di(p-anisyl)tellurium dipropionate 
• 77443-67-5 4-Methoxyphenyltellurium oxochloride 
• 36309-68-9 p-methoxyphenyltellurium trichloride 
• 10026-07-0 tellurium tetrachloride 
• 13139-86-1 4-methoxyphenyl magnesium bromide 
• 39652-02-3 bis(4-methoxyphenyl)-λ⁴-tellanediyl diacetate 
• 57857-69-9 di(p-anisyl)tellurium dibenzoate 
• 98-88-4 benzoyl chloride 
• 79-03-8 propionyl chloride 
• 65683-51-4 C₁₈H₁₄Cl₆O₆Te 
• 57857-68-8 di(p-anisyl)tellurium di(trifluoroacetate) 

Downstream Products

• 57857-68-8 di(p-anisyl)tellurium di(trifluoroacetate) 
• 4456-34-2 bis(4-methoxyphenyl)telluride 
• 613-37-6 4-methoxylbiphenyl 
• 2132-80-1 4,4'-Dimethoxybiphenyl 
• 1694-19-5 E-1-(phenyl)-2-(4'-methoxyphenyl)ethene 
• 42545-43-7 2-(4-methoxyphenyl)thiophene 
• 57857-70-2 di-(p-methoxyphenyl)tellurium oxide 
• 24727-22-8 dibromo-bis-(4-methoxy-phenyl)-λ⁴-tellane 
• 24727-23-9 diiodo-bis-(4-methoxy-phenyl)-λ⁴-tellane 
• 56-89-3 L-cystine 
• 142343-81-5 (CH₃OC₆H₃HgOCOCF₃)2TeCl₂ 
• 1133158-82-3 C₂₀H₁₉ClO₃Te 
• 135302-83-9 C₃₀H₅₀O₆P₂S₄Te 

Relevant articles and documents

Synthesis, Characterization and Antimicrobial Studies of Some New Tellurium(IV) Complexes Derived from 2-[(2-Hydroxyphenyl)imino methyl]-1-naphthol Schiff Base

This article reports the synthesis, characterization and antimicrobial screening of a tridentate 2-[(2-hydroxyphenyl)imino methyl]-1naphthol ligand (H2AP) and its organotellurium(IV) complexes. Structural characterization of the synthesized ligand and com

COMPOSITION FOR RESIST UNDERLAYER FILM FORMATION, UNDERLAYER FILM FOR LITHOGRAPHY, AND PATTERN FORMATION METHOD

The present invention provides a composition for resist underlayer film formation comprising a tellurium-containing compound or a tellurium-containing resin.

The Anticancer Activity of Organotelluranes: Potential Role in Integrin Inactivation

Organic TeIV compounds (organotelluranes) differing in their labile ligands exhibited anti-integrin activities in vitro and anti-metastatic properties in vivo. They underwent ligand substitution with l-cysteine, as a thiol model compound. Unlike inorganic TeIV compounds, the organotelluranes did not form a stable complex with cysteine, but rather immediately oxidized it. The organotelluranes inhibited integrin functions, such as adhesion, migration, and metalloproteinase secretion mediation in B16F10 murine melanoma cells. In comparison, a reduced derivative with no labile ligand inhibited adhesion of B16F10 cells to a significantly lower extent, thus pointing to the importance of the labile ligands of the TeIV atom. One of the organotelluranes inhibited circulating cancer cells in vivo, possibly by integrin inhibition. Our results extend the current knowledge on the reactivity and mechanism of organotelluranes with different labile ligands and highlight their clinical potential.