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VINYLTRIETHYLGERMANE is a colorless, flammable liquid with a distinct, pungent odor, and is a highly reactive chemical compound primarily used as a reagent in organic synthesis.

6207-41-6

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6207-41-6 Usage

Uses

Used in Organic Synthesis:
VINYLTRIETHYLGERMANE is used as a reagent for the production of organic germanium compounds and as a precursor in the synthesis of various other organic compounds.
Used in Pharmaceutical Industry:
VINYLTRIETHYLGERMANE is used as a precursor in the synthesis of pharmaceuticals, contributing to the development of new drugs and medicinal compounds.
Used in Polymer Industry:
VINYLTRIETHYLGERMANE is utilized as a precursor in the synthesis of polymers, which have a wide range of applications in various industries.
Used in Specialty Chemicals:
VINYLTRIETHYLGERMANE is used in the production of specialty chemicals, which are important for specific applications in different fields.
Used in Semiconductor Industry:
It has potential applications in the semiconductor industry, particularly in the production of germanium-based materials for electronic and optoelectronic devices.
It is crucial to handle and store VINYLTRIETHYLGERMANE with caution due to its flammability and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 6207-41-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,0 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6207-41:
(6*6)+(5*2)+(4*0)+(3*7)+(2*4)+(1*1)=76
76 % 10 = 6
So 6207-41-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H18Ge/c1-5-9(6-2,7-3)8-4/h5H,1,6-8H2,2-4H3

6207-41-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name ethenyl(triethyl)germane

1.2 Other means of identification

Product number -
Other names VINYLTRIETHYLGERMANE

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:6207-41-6 SDS

6207-41-6Relevant academic research and scientific papers

Introduction of organogermyl functionalities to cage silsesquioxanes

Fra?ckowiak, Dawid,Grzelak, Magdalena,Januszewski, Rafa?,Marciniec, Bogdan

supporting information, p. 5055 - 5063 (2020/05/13)

In this work, we present the first example of highly efficient platinum-catalyzed hydrosilylation of vinyl- and allylgermanes with different types of silsesquioxanes and spherosilicates. This protocol allows the straightforward introduction of organogermyl functionalities with alkyl chains linked to the silsesquioxane core with good yields and excellent selectivity. These derivatives may be applied as precursors for the development of advanced hybrid materials in the future. In addition, a comparison made between vinylsilanes and vinylgermanes showed a higher reactivity of germanium compounds in the hydrosilylation reaction. To the best of our knowledge, this is the first literature example of the functionalization of silsesquioxanes and spherosilicates with these types of germanium derivatives. The reaction parameters and kinetics were determined by in situ FT-IR. In addition, our research is supported by extensive data obtained from NMR measurements.

New catalytic route to alkynylgermanes

Marciniec, Bogdan,LAwicka, Hanna,Dudziec, Beata

, p. 5188 - 5192 (2008/10/09)

Vinyl-trisubstituted germanes react selectively with terminal alkynes in the presence of compounds containing Ru-H and Ru-Ge bonds with formation of functionalized alkynylgermanes. The reaction opens the first transition metal catalytic route for the preparation of this class of organogermanes, which are useful reagents for organic synthesis. The mechanism elucidated by NMR spectroscopic study of stoichiometric reactions shows that this process is a new catalytic activation of an sp-hybridized C-H bond involving the previously discovered activation of the =C-Ge bond.

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