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Trigermane, 1,1,1,3,3,3-hexamethyl-2,2-diphenyl-, also known as hexamethyl-2,2-diphenyltrigermane, is a chemical compound with the molecular formula C16H24Ge3. It is a derivative of trigermane, which is a germanium-based analog of methane. Trigermane, 1,1,1,3,3,3-hexamethyl-2,2-diphenyl- features a central Ge3 core, with each germanium atom bonded to three methyl groups (CH3) and one phenyl group (C6H5). The presence of phenyl groups in Trigermane, 1,1,1,3,3,3-hexamethyl-2,2-diphenyl- imparts unique electronic and steric properties, making it a subject of interest in organogermanium chemistry. It is typically synthesized through the reaction of germanium tetrachloride with lithium and diphenylmethylmagnesium. Due to its complex structure and potential applications in materials science and organometallic chemistry, hexamethyl-2,2-diphenyltrigermane is a significant compound in the field of inorganic chemistry.

53421-59-3

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53421-59-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53421-59-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,4,2 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 53421-59:
(7*5)+(6*3)+(5*4)+(4*2)+(3*1)+(2*5)+(1*9)=103
103 % 10 = 3
So 53421-59-3 is a valid CAS Registry Number.

53421-59-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name diphenylgermanium,trimethylgermanium

1.2 Other means of identification

Product number -
Other names 1,1,1,3,3,3-hexamethyl-2,2-diphenyltrigermane

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:53421-59-3 SDS

53421-59-3Relevant academic research and scientific papers

Preparation, structural characterization, and reactivities of (digermanyl)lithium. Its application to the synthesis of bis(1,1-dipheny 1-2,2,2-trimethyldigermanyl)platinum(II)

Mochida, Kunio,Ogawa, Satoshi,Naito, Noriaki,El-Al Gaber, Abd,Usui, Yoko,Nanjo, Masato

, p. 414 - 415 (2007/10/03)

(Pentamethyldigermanyl)lithium (Me3GeGeMe2Li, 1a) and (1,1-diphenyl-2,2,2- trimethyldigermanyl)lithium (MeaGeGe-Ph2Li, 1b) were prepared and characterized by spectroscopic methods. The structure of (digermanyl)lithium 1b was established by X-ray diffraction. The reaction of 1b with cis-PtCl 2-(PMe2Ph)2 gave the expected substitution product, transPt(Me3GePh2Ge)2(PMe 2Ph)2. Copyright

Development of novel and efficient synthesis of group 14 element (Ge and Sn) catenates by use of samarium (II) diiodide

Azemi, Takushi,Yokoyama, Yasuo,Mochida, Kunio

, p. 1588 - 1593 (2007/10/03)

Group 14 element catenates such as di-, tri-, poly-germanes, and polystannanes are efficiently synthesized by use of the one-electron reducing agent SmI2 under mild homogeneous conditions in good yields.

The First Application of Samarium(II) Diiodide for the Formation of Group 14 Element Catenates: Synthesis of Tri- or Poly-germanes and Polystannanes

Yokoyama, Yasuo,Hayakawa, Masamichi,Azemi, Takushi,Mochida, Kunio

, p. 2275 - 2276 (2007/10/02)

Some Group 14 element catenates such as tri- or poly-germanes and polystannanes are synthesized by use of the one-electron reducing agent SmI2.

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