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1626-24-0

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1626-24-0 Usage

General Description

Triphenylgermanium chloride, also known as GeCl3Ph3, is a chemical compound that is mainly used in organic and inorganic synthesis. It is a white to off-white crystalline solid that is highly soluble in organic solvents such as benzene and toluene. Triphenylgermanium chloride is a versatile reagent that is often used as a catalyst in a variety of chemical reactions, including the synthesis of polymers and the formation of carbon-carbon bonds. It is also used in the production of pharmaceuticals and agrochemicals. However, it is important to handle triphenylgermanium chloride with care, as it is a hazardous substance that can cause irritation to the skin, eyes and respiratory system.

Check Digit Verification of cas no

The CAS Registry Mumber 1626-24-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,2 and 6 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1626-24:
(6*1)+(5*6)+(4*2)+(3*6)+(2*2)+(1*4)=70
70 % 10 = 0
So 1626-24-0 is a valid CAS Registry Number.
InChI:InChI=1/C18H15ClGe/c19-20(16-10-4-1-5-11-16,17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15H

1626-24-0 Well-known Company Product Price

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  • Aldrich

  • (288217)  Triphenylgermaniumchloride  99%

  • 1626-24-0

  • 288217-5G

  • 1,862.64CNY

  • Detail

1626-24-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name TRIPHENYLGERMANIUM CHLORIDE

1.2 Other means of identification

Product number -
Other names chloro(triphenyl)germane

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:1626-24-0 SDS

1626-24-0Relevant articles and documents

Studies of germanium-platinum bonds in bis(aryl-substituted germyl)platinum complexes by laser flash photolysis and chemical trapping experiments

Mochida, Kunio,Masukawa, Yusuke,Yamada, Atsuko,Yanaga, Mai,Nanjo, Masato,Arii, Hidekazu,Gohdo, Masao,Wakasa, Masanobu

, p. 62 - 63 (2008)

The UV photolysis of bis(triaryl-substituted germyl)platinum complexes, Pt(Ar3Ge)2(PMe2Ph)2 (Ar = Ph, p-C6H4-SiMe3, and p-C6H 4C(CH3)3

Iron-catalyzed chlorination of silanes

Savela, Risto,Zawartka, Wojciech,Leino, Reko

, p. 3199 - 3206 (2012/06/04)

A simple and highly efficient iron-catalyzed method for the chlorination of silanes has been developed. By use of 0.5-2% of the Fe(III)-based catalyst FeCl3 or Fe(acac)3 in the presence of 1-1.5 equiv of acetyl chloride as the chlorine donor, a large number of silanes, alkoxysilanes, and silanols were converted to the corresponding chlorosilanes in 50-93% yields. In contrast to earlier reported methods often suffering from expensive catalysts or use of stoichiometric metal salts, hazardous reagents, and reaction conditions, the presently described methodology allows benign reaction conditions and simple workup while using only catalytic amounts of a readily available and economically viable iron catalyst.

Reactions of organochlorosilanes with chloro-and organogermanes in the presence of aluminum chloride

Zhun,Sbitneva,Polivanov,Chernyshev

, p. 1564 - 1570 (2008/02/09)

The effect of substituents at the silicon and germanium atoms in reactions of organochlorosilanes with chloro-and organogermanes in the presence of aluminum chloride was studied. The only occurring process is the exchange of the chlorine atoms at Ge for the phenyl groups from Si; an increase in the number of methyl groups or chlorine atoms at Si promotes formation of phenyltrichlorogermane, and an increase in the number of phenyl groups or replacement of the chlorine atom at the Si atom by hydrogen leads to the formation of di-and triphenylchlorogermanes. Neither phenyl nor other radicals are transferred back from Ge to Si in the course of reactions of phenylgermanes with methylchlorosilanes in the presence of aluminum chloride; the only occurring processes are the exchange of the phenyl or methyl radicals bonded to Ge for the Cl atom bonded to Al and the disproportionation of phenylchlorogermanes. Nauka/Interperiodica 2006.

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