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Phenyltribromogermane, also known as bromophenylgermane, is an organogermanium compound with the chemical formula C6H5GeBr3. It is a colorless, crystalline solid that is sensitive to light and moisture. phenyltribromogermane is formed by the reaction of benzene with tribromogermane, and it is used as a precursor in the synthesis of various organogermanium compounds. Phenyltribromogermane is also employed as a reagent in organic synthesis, particularly in the formation of carbon-carbon bonds and the introduction of germanium-containing groups into organic molecules. Due to its reactivity and potential applications in materials science and pharmaceuticals, phenyltribromogermane is a subject of ongoing research in the field of organometallic chemistry.

1074-28-8

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1074-28-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1074-28-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,7 and 4 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1074-28:
(6*1)+(5*0)+(4*7)+(3*4)+(2*2)+(1*8)=58
58 % 10 = 8
So 1074-28-8 is a valid CAS Registry Number.

1074-28-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name phenyltribromogermane

1.2 Other means of identification

Product number -
Other names Phenyl-tribromogerman

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:1074-28-8 SDS

1074-28-8Downstream Products

1074-28-8Relevant academic research and scientific papers

Microwave-assisted Lewis acid catalysis: Application to the synthesis of alkyl- or arylhalogermanes

Laurent, Régis,Laporterie, André,Dubac, Jacques,Berlan, Jacques

, p. 2493 - 2495 (2008/10/08)

Under microwave irradiation, alkyl- or arylhalogermanes RnGeX4-n (R = Et, Bu, Ph; X = Cl, Br) are obtained by redistribution reactions of R4Ge with GeX4. These experimental conditions permit the synthesis of such compounds in good yield in a few minutes at atmospheric pressure. The direct Friedel-Crafts germylation of benzene and toluene by germanium tetrachloride also has been performed, but yields were low.

SYNTHESE DE COMPOSES A LIAISON MIVB-MERCURE. PRECURSEURS D'ESPECES MONOVALENTES (GERMYNES), ET BIVALENTES (GERMYLENES), DE RADICAUX CENTROMETALLES ET D'INTERMEDIAIRES

Riviere, P.,Castel, A.,Satge, J.

, p. 351 - 367 (2007/10/02)

Polynuclear germyl-mercury compounds are obtained from the reaction of organohydrogermanes PhnGeH4-n or digermanes Ph2nGe2H4-n (n = 1, 2) with dialkylmercury R2Hg.Di- or tri-mercurated geminal polygermates thus synthesized generally present a low stability and undergo thermal- or photodecompositions leading to the corresponding monovalent (germynes), divalent (germylenes) or, trivalent (germanium centered radicals) species and also to intermediate biradicals which could be considered as limit forms of germanium doubly-bonded compounds .Such intermediates have been chemically and spectroscopically characterized.Extension of these reactions to the silicon analogs met with difficulties, and thus previously observed differences between silicon and germanium chemistry were confirmed.

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