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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

Reaction of germanes and digermanes with triflic acid: The route to novel organooligogermanes

Zaitsev, Kirill V.,Kapranov, Andrey A.,Oprunenko, Yuri F.,Churakov, Andrei V.,Howard, Judith A.K.,Tarasevich, Boris N.,Karlov, Sergey S.,Zaitseva, Galina S.

, p. 207 - 213 (2012/03/26)

Novel germanium containing triflates were prepared from the reactions of trifluoromethanesulfonic acid with tetraphenylgermane (1) and digermanes (Ph3GeGeMe3 (4), Ph3GeGePh3 (5)). The improved procedures for synthesis of known organogermanium compounds (Ph4Ge (1), Ph3GeCl (2), Ph3GeGeMe3 (4), Ph3GeGePh3 (5)) were also presented. The crystal structure of Ph3GeOTf (6) and Ph2Ge(OTf)Ge(OTf)Ph 2 (7) was studied by X-ray analysis. In 7 each germanium atom is pentacoordinated due to intramolecular interaction with O atom of the neighboring triflate group.

Preparation, structural characterization, and photochemical reactions of silyl- and germylborates

Nanjo, Masato,Matsudo, Kazuhiko,Kurihara, Mari,Nakamura, Sayaka,Sakaguchi, Yoshio,Hayashi, Hisaharu,Mochida, Kunio

, p. 832 - 838 (2008/10/09)

Silylborates (Li[PhnMe3-nSiBPh3], n = 1-3) and germylborates (Li[PhnMe3-nGeBPh3], n = 1-3; M[Et3- GeBPh3], M = Li, Na, K) were prepared by the reaction of the corresponding silyl- and germylalkali metals with triphenylborane in a hexane/benzene mixed solvent. The silyl- and germylborates were fully identified by 1H, 13C, 11B, and 7Li NMR spectroscopic methods. The solid-state structure of germylborates Li[Ph3GeBPh3] and M[Et3GeBPh 3] (M = Li and Na) were determined by X-ray diffraction analyses. The polymeric structure of M[Et3GeBPh3] was observed in the solid state and in hydrocarbon solution. The alkali metal atoms were located near the center of the benzene ring of triphenylborane and interacted with the neighboring borate molecules by Li+-π interaction. The polymeric structure was broken by the addition of MeOH. However, M[Et 3GeBPh3] was coordinated by three MeOH molecules to form a dimeric structure without methanolysis reaction. The primary processes in photochemical reactions of silyl- and germylborates were investigated by chemical trapping experiments and the CIDEP (chemical-induced dynamic electron polarization) method. The cleavage of the Ge-B (or Si-B) bonds of germylborates (or silylborates) was considered most probably to occur from their triplet states.

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