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1,3,2,4-Dithiadiplumbetane, 2,2,4,4-tetrakis[2,4,6-tris(1-methylethyl)phenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

163852-40-2

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163852-40-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 163852-40-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,3,8,5 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 163852-40:
(8*1)+(7*6)+(6*3)+(5*8)+(4*5)+(3*2)+(2*4)+(1*0)=142
142 % 10 = 2
So 163852-40-2 is a valid CAS Registry Number.

163852-40-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,4,4-tetrakis(2,4,6-triisopropylphenyl)-1,3,4,2,5-dithiadiplumbetane

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

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

More Details:163852-40-2 SDS

163852-40-2Downstream Products

163852-40-2Relevant academic research and scientific papers

Synthesis, structure, and reactivity of kinetically stabilized divalent organolead compounds (plumbylenes)

Kano, Naokazu,Shibata, Kazusato,Tokitoh, Norihiro,Okazaki, Renji

, p. 2999 - 3007 (2008/10/08)

Divalent organolead compounds (plumbylenes; Tip2Pb (6; Tip = 2,4,6-triisopropylphenyl) and Tbt(R)Pb (7a, R = Tbt; Tb, R = Ttm; 7c, R = Tip; 7d, R = Dis; Tbt = 2,4,6-tris[bis-(trimethylsilyl)methyl]phenyl, Ttm = 2,4,6-tris[(trimethylsilyl)methyl]phenyl, and Dis = bis-(trimethylsilyl)methyl)) were synthesized by taking advantage of kinetic stabilization afforded by bulky substituents and characterized by UV/vis and 207Pb NMR spectroscopy. X-ray structural analysis revealed that plumbylene 7a has a V-shaped, monomeric structure. Reactions of these plumbylenes with methyl iodide, carbon tetrabromide, diphenyl disulfide, diphenyl diselenide, and elemental sulfur are described. New methods for the synthesis of plumbylenes from tetravalent organolead compounds, by reductive debromination of dibromoplumbanes and exhaustive desulfurization of tetrathiaplumbolanes, were developed.

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