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Benzenethiol, 4-chloro-, lead(2+) salt (2:1) is a chemical compound with the formula C6H4ClS·Pb. It is a derivative of benzenethiol, where one of the hydrogen atoms is replaced by a chlorine atom, and it forms a salt with lead(2+) ions in a 2:1 ratio. Benzenethiol,4-chloro-, lead(2+) salt (2:1) is an organolead compound, which is a type of organometallic compound that contains carbon-lead bonds. It is important to note that organolead compounds, including this one, are toxic and have been associated with severe health and environmental risks. Due to their toxicity, the use of organolead compounds has been largely phased out, particularly in applications such as gasoline additives. The compound is typically synthesized for research purposes or as an intermediate in the production of other chemicals.

32812-93-4

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32812-93-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 32812-93-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,8,1 and 2 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 32812-93:
(7*3)+(6*2)+(5*8)+(4*1)+(3*2)+(2*9)+(1*3)=104
104 % 10 = 4
So 32812-93-4 is a valid CAS Registry Number.

32812-93-4SDS

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 4-chlorobenzenethiol,lead

1.2 Other means of identification

Product number -
Other names -

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

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:32812-93-4 SDS

32812-93-4Relevant academic research and scientific papers

Synthesis, Structure, and Catalytic Activity of μ-Alkylthio- and μ-Arylthio-μ-chloro-dicarbonylbis(tri-tert-butylphosphane)dirhodium Complexes

Schumann, Herbert,Cielusek, Guy,Jurgis, Stanislaw,Hahn, Ekkehardt,Pickardt, Joachim,et al.

, p. 2825 - 2838 (2007/10/02)

Tetracarbonyldi-μ-chloro-dirhodium (1) reacts with tri-tert-butylphosphane and alkyl or aryl trimethylsilyl sulfides 4 to give complexes tBu3)2Cl(SR)> (5a-i).The complexes 5h,i with the surface active trialkoxysilyl groups are fixed onto a fused silica support.The X-ray structural analyses of tBu3)2Cl(StBu)> (5c) and tBu3)2Cl(SC6H4Cl)> (5g) indicate a cis-configuration of the tri-tert-butylphosphane ligands.The new complexes catalyze the isomerization of 1-octen-3-ol (10) into 3-octanone (11), of 4-allylanisole (12) into cis- and trans-4-(1-propenyl)anisole (13), of trans-stilbene oxide (14) into desoxybenzoin (15), the transfer hydrogenation of α,β-unsaturated ketones by formic acid (16 -> 17), and the transfer hydrogenolysis of trihalomethyl compounds (18, 20) by halogen free alcohols.

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