51112-72-2 Usage
Uses
Used in Organic and Medicinal Chemistry:
DiisopropylTelluride is used as a precursor for the synthesis of organotellurium compounds, which are important in organic and medicinal chemistry. These organotellurium compounds exhibit unique chemical properties and reactivity, making them valuable for the development of new pharmaceuticals and organic materials.
Used in Polymer Synthesis:
DiisopropylTelluride is utilized as a reagent in the preparation of tellurium-containing polymers. These polymers have potential applications in various industries, including electronics, where they can be used in the development of new materials with unique electrical and optical properties.
Used in Semiconductor Material Production:
In the semiconductor industry, DiisopropylTelluride is employed in the production of semiconductor materials. Tellurium and its compounds are known for their electronic properties, making them suitable for use in the fabrication of semiconductor devices.
Used in Catalytic Reactions:
DiisopropylTelluride has been studied for its potential role in catalytic reactions. Its unique chemical properties allow it to act as a catalyst, facilitating various chemical transformations and improving the efficiency of chemical processes.
Used as a Stabilizing Agent for Metal Nanoparticles:
DiisopropylTelluride has also been investigated for its use as a stabilizing agent for metal nanoparticles. DiisopropylTelluride can help prevent the aggregation of nanoparticles, which is crucial for maintaining their desired properties and performance in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 51112-72-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,1,1 and 2 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 51112-72:
(7*5)+(6*1)+(5*1)+(4*1)+(3*2)+(2*7)+(1*2)=72
72 % 10 = 2
So 51112-72-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H14Te/c1-5(2)7-6(3)4/h5-6H,1-4H3
51112-72-2Relevant academic research and scientific papers
REACTIONS OF CHALCOGENS WITH ACETYLENES. ALKYL VINYL TELLURIDES FROM TELLURIUM, ACETYLENE, AND ALKYL HALIDES
Gusarova, N. K.,Trofimov, B. A.,Tatarinova, A. A.,Potapov, V. A.,Sinegovskaya, L. M.,at al.
, p. 1686 - 1691 (2007/10/02)
Methods were developed for the synthesis of alkyl vinyl tellurides from metallic tellurium, acetylene, and alkyl halides in the KOH-SnCl2-H2O system and also by the successive action of lithium and alkyl halide on divinyl telluride in liquid ammonia.
ALKYLVINYL TELLURIDES FROM TELLURIUM, ACETYLENE AND ALKYL HALIDES
Trofimov, B. A.,Gusarova, N. K.,Tatarinova, A. A.,Potapov, V. A.,Sinegovskaya, L. M.,et. al.
, p. 6739 - 6744 (2007/10/02)
Synthetic routes to alkylvinyl tellurides by direct reaction of metallic tellurium, acetylene and alkyl halide in the system KOH-SnCl2-H2O and successive interaction of divinyl telluride with lithium and alkyl halide in liquid ammonia have been developed.
TELLUROPHOSPHONIUM-KATIONEN
Kuhn, Norbert,Schumann, Hans
, p. 199 - 202 (2007/10/02)
Tellurophosphoranes R3P=Te (R = CH3, i-C3H7, n-C4H9, t-C4H9, N(CH3)2) 1 react with CH3I to give the cations + 2.Te(CH3)2 and R3P are formed on treatment of 2 with LiCH3.
