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1153-06-6

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1153-06-6 Usage

General Description

Triphenyllead chloride is a chemical compound that is composed of lead, chlorine, and phenyl groups. It is a highly toxic and dangerous substance that is used primarily as a stabilizer in polyvinyl chloride (PVC) plastics and as a catalyst in organic reactions. Exposure to triphenyllead chloride can cause serious health effects, including damage to the nervous system, kidneys, and reproductive organs. It is also known to be a respiratory and skin irritant, and can have long-lasting negative effects on the environment. Due to its toxicity and potential for harm, the use and production of triphenyllead chloride has been limited and regulated in many countries.

Check Digit Verification of cas no

The CAS Registry Mumber 1153-06-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,5 and 3 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1153-06:
(6*1)+(5*1)+(4*5)+(3*3)+(2*0)+(1*6)=46
46 % 10 = 6
So 1153-06-6 is a valid CAS Registry Number.
InChI:InChI=1/3C6H5.ClH.Pb/c3*1-2-4-6-5-3-1;;/h3*1-5H;1H;/q;;;;+1/p-1/rC18H15ClPb/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

1153-06-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name chloro(triphenyl)plumbane

1.2 Other means of identification

Product number -
Other names triphenyl-lead chloride

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:1153-06-6 SDS

1153-06-6Relevant articles and documents

Hypercoordinated eka-tin materials with dangling aryl-methoxy and -methylthio ligands exhibiting intramolecular secondary bonding and aryl bond stabilization in reactions with organotin chlorides

Arias-Ugarte, Renzo,Metta-Maga?a, Alejandro J.,Ornelas, Alfredo,Pannell, Keith H.,Sharma, Hemant K.

, p. 16084 - 16091 (2021/11/27)

The syntheses of [2-(CH3ECH2)C6H4]PbPh3-nCln, (n = 0, E = O (4), E = S (5); n = 1, E = O (6), E = S (7); n = 2, E = O (8), are described. NMR and single crystal data illustrate significant Pb?E interactions increasing as n progresses from 0 to 2. The Pb?E interactions stabilize the Pb-aryl bonding to the extent that the reactions of 4 and 5 with Me2SnCl2 result in interchange of a Ph group and Cl to produce 6 and 7, respectively, together with Me2PhSnCl. This journal is

Synthesis, properties and application of electronically-tuned tetraarylarsonium salts as phase transfer catalysts (PTC) for the synthesis of gem-difluorocyclopropanes

Grudzień, Krzysztof,Basak, Tymoteusz,Barbasiewicz, Micha?,Wojciechowski, Tomasz M.,Fedoryński, Micha?

supporting information, p. 106 - 110 (2017/04/11)

Preparation of gem-difluorocyclopropane from α-methylstyrene and chlorodifluoromethane was investigated under basic two-phase conditions. Although simple tetraalkylammonium salts appeared uneffective as phase-transfer catalysts (PTC) for this purpose, tetraphenylarsonium chloride displayed moderate activity, and inspired studies of the phenomena. To improve its efficiency we synthesized set of electronically-tuned tetraarylarsonium analogues. Their preparation revealed interesting exchange process of aryl substituents on the arsonium center, whereas activity studies demonstrated a correlation of catalytic efficiency with electronic effects of the substituents. Two of the tetraarylarsonium catalysts were characterized by X-ray studies.

Versatile reagent Ph3As(OTf)2: One-pot synthesis of [P7(AsPh3)3][OTf]3 from PCl3

Donath, Maximilian,Bodensteiner, Michael,Weigand, Jan J.

supporting information, p. 17306 - 17310 (2015/02/19)

Compound Ph3As(OTf)2 as a pentacoordinated AsV Lewis acid readily forms dicationic Lewis acid/base ad-ducts upon addition of various Lewis bases. It also represents a stronger chloride-abstracting agent than Me3SiOTf and facilitates the reductive coupling of PCl3 in the presence of AsPh3 to the unprecedented cation [P7(AsPh3)3]3+ as triflate salt. This crystallographically characterized nor-tricyclane-type cation represents a P7R3-derivative with the most electron-withdrawing substituents, resulting in a pronounced effect on the structural parameters of the P7 core.

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