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2117-71-7

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2117-71-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2117-71-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,1 and 7 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2117-71:
(6*2)+(5*1)+(4*1)+(3*7)+(2*7)+(1*1)=57
57 % 10 = 7
So 2117-71-7 is a valid CAS Registry Number.

2117-71-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name diphenylgermanium

1.2 Other means of identification

Product number -
Other names octaphenyl-cyclo tetragermane

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:2117-71-7 SDS

2117-71-7Relevant articles and documents

Kraus,Brown

, p. 4031,4034 (1930)

Reductive Coupling Reactions of Dihalogenogermanes with Magnesium and Magnesium Bromide: Simple Preparation of Cyclotrigermanes and Cyclotetragermanes

Ando, Wataru,Tsumuraya, Takeshi

, p. 1514 - 1515 (2007/10/02)

The reactions of various dihalogenogermanes with Mg and MgBr2 in tetrahydrofuran produce the corresponding cyclotrigermanes and cyclotetragermanes; the ring size of the products depends on the steric bulk of substituents on germanium.

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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