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1520-78-1

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1520-78-1 Usage

General Description

Trimethyl Lead Chloride is a chemical substance with the formula (CH3)3PbCl. It's an organolead compound, a branch of organic chemistry that deals with organometallic compounds consisting of lead. It's obtained through the mixing of Grignard reagents with lead halides under specific conditions. As a highly toxic substance, its use and handling are highly regulated. It is essential to consider safety measures during its handling because of its detrimental health and environmental effects. Symptoms linked with Trimethyl Lead Chloride exposure include headaches, memory loss, and weakness. TRIMETHYL LEAD CHLORIDE is mainly used in labs for research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 1520-78-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,2 and 0 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1520-78:
(6*1)+(5*5)+(4*2)+(3*0)+(2*7)+(1*8)=61
61 % 10 = 1
So 1520-78-1 is a valid CAS Registry Number.
InChI:InChI=1/3CH3.ClH.Pb/h3*1H3;1H;/q;;;;+1/p-1/rC3H9ClPb/c1-5(2,3)4/h1-3H3

1520-78-1SDS

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(trimethyl)plumbane

1.2 Other means of identification

Product number -
Other names 1&Chlorotrimethyllead

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:1520-78-1 SDS

1520-78-1Relevant articles and documents

Pant,Davidson

, p. 295,297 (1972)

Holliday,Jessop

, p. 889 (1967)

Trifluoromethylsubstituierte Plumbane. Synthese, Eingeschaften und NMR-Spektren der Verbindungen (CF3)nPbR4-n (n = 1-3) und (CF3)nPbR3-nX (n = 1, 2; R = Me, Et; X = Hal)

Eujen, R.,Patorra, A.

, p. 57 - 75 (2007/10/02)

Trifluoromethylated derivatives of lead, (CF3)nPbR4-n (n = 1-3; R = CH3, C2H5), have been prepared by a stepwise halide/CF3 exchange from (CF3)nPbR3-nX (n = 0-2) and donor-stabilized (CF3)2Cd.Upon treatment of CF3PbR3 and (CF3)2PbR2 with halides under mild conditions, selective cleavage of the Pb-C(H) bond and formation of the corresponding alkyl(trifluoromethyl)haloplumbanes were achieved, whereas with (CF3)3PbMe only (CF3)2PbMeX was obtained.The direct exchange of alkyl and trifluoromethyl groups was observed for the systems PbR4/(CF3)nE (E = Hg, Ge, Sn), (CF3)4Sn being the most efficient CF3 transfer reagent.All compounds were characterized by vibrational, mass and multinuclear NMR spectroscopy.The NMR coupling constants nJ(207Pb-E) (E = 19F, 1H, 13C), which vary strongly with solvents and substituents, have been determined along with their absolute sings.Linear correlations found between 1J(207Pb-CF3) and 2J(207Pb-F) or 2J(207Pb-F) and 2J(119Sn-F) of homologous trifluoromethylated stannanes, respectively.

Sulfur-Nitrogen Compounds, IX Preparation and Spectroscopical Characterization of Some Sulfur Diimines with Elements of Main Group IV

Brands, G.,Golloch, A.

, p. 568 - 573 (2007/10/02)

Compounds of the sulfur(IV) diimines with elements of the main group IVb were prepared.Spectroscopic behaviour and the scope and limitations of preparing sulfurdiimines from amines and N3S3Cl3 are discussed. - Key words: Sulfurdiimines, Trithiazyltrichloride

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