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Tetraallylgermane, with the molecular formula C12H20Ge, is a colorless to pale yellow liquid chemical compound. It is insoluble in water but soluble in organic solvents. TETRAALLYLGERMANE serves as a crucial precursor in the synthesis of various organogermanium compounds, which are utilized in a range of applications including semiconductor production, polymerization catalysts, and pharmaceutical intermediates. Additionally, it finds use in the formulation of coatings, adhesives, and sealants. Due to its toxic nature upon ingestion or inhalation, and potential to cause skin and eye irritation, Tetraallylgermane requires careful handling and use with appropriate safety measures.

1793-91-5

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1793-91-5 Usage

Uses

Used in Semiconductor Industry:
Tetraallylgermane is used as a precursor for the synthesis of organogermanium compounds, which are essential in the production of semiconductors. These compounds contribute to the development of electronic devices and components.
Used in Chemical Catalysts Industry:
In the field of chemical catalysis, Tetraallylgermane serves as a starting material for the creation of polymerization catalysts. These catalysts are vital for accelerating chemical reactions in the production of various polymers.
Used in Pharmaceutical Industry:
As a pharmaceutical intermediate, Tetraallylgermane plays a significant role in the development of new drugs. Its derived organogermanium compounds may possess unique properties that can be harnessed for therapeutic applications.
Used in Coatings, Adhesives, and Sealants Industry:
Tetraallylgermane is also utilized in the formulation of coatings, adhesives, and sealants, where its organogermanium compounds can enhance the performance characteristics of these materials, such as adhesion, durability, and resistance to environmental factors.

Check Digit Verification of cas no

The CAS Registry Mumber 1793-91-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,9 and 3 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1793-91:
(6*1)+(5*7)+(4*9)+(3*3)+(2*9)+(1*1)=105
105 % 10 = 5
So 1793-91-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H20Ge/c1-5-9-13(10-6-2,11-7-3)12-8-4/h5-8H,1-4,9-12H2

1793-91-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name TETRAALLYLGERMANE

1.2 Other means of identification

Product number -
Other names tetraallyl germane

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1793-91-5 SDS

1793-91-5Relevant academic research and scientific papers

Reactivity of dianionic hexacoordinate germanium complexes toward organometallic reagents. A new route to organogermanes

Cerveau,Chuit,Corriu,Reyé

, p. 1510 - 1515 (2008/10/08)

Lithium and potassium tris(benzene-1,2-diolato)germanates (2a and 2b, respectively) and potassium tris(butane-2,3-diolato)germanate (3) are easily prepared from GeO2 in quantitative yields. They are very reactive toward organometallic reagents, the reactivity depending on the ligands on the germanium. Complexes 2 react with an excess of Grignard reagent to give the corresponding tetraorganogermanes R4Ge while the less reactive complex 3 leads to the functional triorganogermanes R3GeX. Tetraorganogermanes can also be prepared from complex 2b by reaction with organic bromides in the presence of Mg (Barbier reaction). The influence of Cp2TiCl2 and MgBr2 on the reactivity of Grignard reagents with these complexes was also investigated: in both cases formation of triorganogermanes was favored.

Reactions of nucleophilic reagents with dianionic hexacoordinated germanium complexes: A new convenient route to functional organogermanes from germanium dioxide

Cerveau,Chuit,Corriu,Reye

, p. 786 - 787 (2008/10/08)

Tetraorganogermanes and triorganogermanes can be prepared in two steps from GeO2: the preparation of the anionic hexacoordinated germanium complexes followed by reaction of these with Grignard reagents to give the organogermanes.

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