1067-10-3 Usage
Description
BROMOTRIETHYLGERMANE, also known as Triethylgermanium Bromide, is an organic bromide compound that serves as a versatile reagent, catalyst, and precursor material in various industries. It is characterized by its unique chemical properties and wide-ranging applications, making it a valuable component in the fields of thin film deposition, industrial chemistry, pharmaceuticals, and LED manufacturing.
Uses
Used in Thin Film Deposition:
BROMOTRIETHYLGERMANE is used as a precursor material for thin film deposition, allowing for the creation of high-quality films with desired properties. Its use in this application is due to its ability to form stable and uniform films, which are essential for various applications in the electronics and optoelectronics industries.
Used in Industrial Chemistry:
In the realm of industrial chemistry, BROMOTRIETHYLGERMANE is utilized as a catalyst to enhance the efficiency and selectivity of various chemical reactions. Its use in this application is attributed to its ability to facilitate specific reaction pathways, leading to improved product yields and reduced environmental impact.
Used in Pharmaceuticals:
BROMOTRIETHYLGERMANE is employed as a reagent in the pharmaceutical industry, particularly for the formation of dienolates of α, β-unsaturated esters. Its use in this application is due to its ability to promote specific chemical transformations, which are crucial for the synthesis of various pharmaceutical compounds.
Used in LED Manufacturing:
In the LED manufacturing industry, BROMOTRIETHYLGERMANE is used as a precursor material for the production of high-performance light-emitting diodes. Its use in this application is attributed to its ability to contribute to the formation of efficient and durable LED structures, which are essential for energy-saving and eco-friendly lighting solutions.
Used in Methylenecyclopentane Annulation Reactions:
BROMOTRIETHYLGERMANE is also used as a reagent in methylenecyclopentane annulation reactions, which are important for the synthesis of complex organic molecules. Its use in this application is due to its ability to facilitate the formation of cyclic structures, which are often found in various biologically active compounds and materials with unique properties.
Check Digit Verification of cas no
The CAS Registry Mumber 1067-10-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,6 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1067-10:
(6*1)+(5*0)+(4*6)+(3*7)+(2*1)+(1*0)=53
53 % 10 = 3
So 1067-10-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H15BrGe/c1-4-8(7,5-2)6-3/h4-6H2,1-3H3
1067-10-3Relevant articles and documents
Palladium complex-catalyzed germylation of allylic halides using (germyl)stannanes
Nakano, Taichi,Ono, Kazuyoshi,Senda, Yoshiya,Migita, Toshihiko
, p. 313 - 317 (2007/10/03)
(Triethylgermyl)tributylstannane reacts metal-selectively with allylic halides at room temperature (r.t.) in the presence of tris(dibenzylideneacetone)dipalladium, Pd2(dba)3CHCl3, to provide an alternative route to allylge
METAL-HALOGEN BONDING STUDIES WITH GROUP IV A TRIALKYLMETAL HALIDES
Friedrich, Edwin C.,Abma, Charles B.,Vartanian, Paul F.
, p. 203 - 212 (2007/10/02)
Halogen redistribution reactions have been found to take place between benzyl bromide or benzyl iodide and the Group IV A silicon, germanium, tin, and lead containing trialkylmetal chlorides.However, for the reactions of the Si, Ge and Sn compounds, a quaternary ammonium halide catalyst was necessary to enable the equilibria to be established at reasonably rapid rates.The equilibrium constants at 50 deg C have been measured for each of these halogen redistributions.They have been found to increase gradually on going down in Group IV A from silicon to lead, being conside rably less than unity in the case of silicon and somewhat greater than unity in the case of lead for both the R3MCl + BzBr and R3MCl + BzI reactions.The ΔG0 values for these equilibria have been calculated, and it is suggested that their differences may be explained in terms of the relative importance of p?-d? contributions to the halogen-metal bonding in the various Group IV A trialkylmetal halide systems.
