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Trimethyl(2-furyl)germane is an organogermanium compound with the chemical formula C7H12GeO. It is a colorless liquid at room temperature and is characterized by its distinct odor. trimethyl(2-furyl)germane is formed by the combination of a trimethylgermanium group (Ge(CH3)3) and a 2-furyl group (C4H3O), which is a heterocyclic aromatic ring containing an oxygen atom. Trimethyl(2-furyl)germane is synthesized through the reaction of 2-furan with trimethylgermanium bromide in the presence of a base. It is used in various applications, including as a precursor in the synthesis of other organogermanium compounds and as a reagent in organic chemistry. Due to its reactivity and potential toxicity, it is essential to handle trimethyl(2-furyl)germane with care, following appropriate safety protocols.

55811-72-8

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55811-72-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55811-72-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,8,1 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 55811-72:
(7*5)+(6*5)+(5*8)+(4*1)+(3*1)+(2*7)+(1*2)=128
128 % 10 = 8
So 55811-72-8 is a valid CAS Registry Number.

55811-72-8Relevant academic research and scientific papers

Photochemical reactions of 2-(pentamethyldisilanyl)furan and 2-(pentamethyldigermanyl)furan. Formation of a radical pair

Mochida, Kunio,Kimijima, Kohichi,Wakasa, Masanobu,Hayashi, Hisaharu

, p. 101 - 108 (1994)

Photochemical reactions of 2-(pentamethyldisilanyl)furan and 2-(pentamethyldigermanyl)furan have been investigated by chemical trapping experiments and laser flash-photolysis.On irradiation, the furylated catenates of Group 14 elements undergo silicon-silicon ? bond and germanium-germanium ? bond homolysis to give a pair of silyl radicals and germyl radicals, respectively.In CCl4, these radicals are converted to the corresponding chlorides by abstraction of a chlorine atom.In nonhalogenated solvents (cyclohexane and other hydrocarbons), the silyl radical pair undergoes a disproportionation to give as main products a monosilane and a silene.The trimethylgermyl radical mainly couples at the ipso-position of the furyl group of the pairing radical to yield the corresponding diradical.This diradical undergoes elimination of a divalent species, dimethylgermylene, with concomitant formation of 2-(trimethylgermyl)furan. Key words: Photochemistry; Silanyl; Germanyl; Radical

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