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Trimethyl(naphthalen-1-yl)germane is an organogermanium compound characterized by the presence of a germanium atom bonded to three methyl groups and a naphthalen-1-yl group. trimethyl(naphthalen-1-yl)germane is a derivative of naphthalene, a polycyclic aromatic hydrocarbon, with a germanium atom replacing one of the hydrogen atoms on the naphthalene ring. The chemical structure of trimethyl(naphthalen-1-yl)germane can be represented as C13H15Ge, indicating its molecular composition of 13 carbon, 15 hydrogen, and 1 germanium atoms. trimethyl(naphthalen-1-yl)germane is of interest in the field of organometallic chemistry, where it may be studied for its unique electronic properties and potential applications in materials science.

31608-60-3

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31608-60-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 31608-60-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,6,0 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 31608-60:
(7*3)+(6*1)+(5*6)+(4*0)+(3*8)+(2*6)+(1*0)=93
93 % 10 = 3
So 31608-60-3 is a valid CAS Registry Number.

31608-60-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name trimethyl(naphthalen-1-yl)germane

1.2 Other means of identification

Product number -
Other names Germane,trimethyl-1-naphthalenyl

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:31608-60-3 SDS

31608-60-3Downstream Products

31608-60-3Relevant academic research and scientific papers

Photochemical reactions of digermanyl-substituted naphthalenes: The germyl migration to the aromatic ring

Mochida, Kunio,Ginyama, Hiroyuki,Takahashi, Masae,Kira, Mitsuo

, p. 163 - 171 (2007/10/03)

Photochemical reactions of digermanyl-substituted naphthalenes have been investigated by chemical studies using trapping agents, laser flash photolysis, and ab initio MO calculations. Irradiation of 1-(pentamethyldigermanyl)naphthalene (1) afforded mainly an isomer, 1-(dimethylgermyl)-8-(trimethylgermyl)naphthalene (4), via photochemical formation of a pair of trimethylgermyl radical and 1- naphthyldimethylgermyl radical, and then recombination at the 8-position of the latter followed by an intramolecular 1,4-hydrogen shift. At the same time a small amount of 1-(trimethylgermyl)naphthalene (5) was formed through the dimethylgermylene extrusion from 1. From photolysis of 2-(pentamethyldigermany)naphthalene a high molecular weight polymer was obtained. The excited states of digermanyl-substituted naphthalenes responsible for the photodecomposition are also discussed.

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