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Stannane, 1,3-propanediylbis[triphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

86623-72-5

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86623-72-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86623-72-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,6,2 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 86623-72:
(7*8)+(6*6)+(5*6)+(4*2)+(3*3)+(2*7)+(1*2)=155
155 % 10 = 5
So 86623-72-5 is a valid CAS Registry Number.

86623-72-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name triphenyl(3-triphenylstannylpropyl)stannane

1.2 Other means of identification

Product number -
Other names 1,3-Bis-triphenylstannyl-propan

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:86623-72-5 SDS

86623-72-5Relevant academic research and scientific papers

Synthesis and characterization of silicon-based group 14 dendrimers Si{(CH2)2Sn[(CH2)4MPh 3]3}4 (M = Ge, Sn)

Schumann, Herbert,Aksu, Yilmaz

, p. 397 - 402 (2008/10/09)

The catalytic hydrogermylation of Si(CH=CH2)4 with Ph3GeH yielded Si(CH2CH2GePh3) 4 (1). In contrast, Sn(CH=CH2)4 and Sn(CH 2CH=CH2)s

Synthesis and characterization of some organo-all-tin dendrimers with different peripheral substituents

Schumann, Herbert,Aksu, Yilmaz,Wassermann, Birgit C.

, p. 1703 - 1712 (2007/10/03)

The synthesis of the first all-tin-dendrimer Sn[(CH2) 4SnPh3]4 (2) results from complete hydrostannation of tetra(but-3-enyl)stannane (1) with triphenyltin hydride. Selective cleavage of one phenyl group from ea

Synthesis, NMR studies and molecular structures of 2 and 2(S)(CH2)3

Dakternieks, Dainis,Jurkschat, Klaus,Schollmeyer, Dieter,Wu, Hong

, p. 145 - 150 (2007/10/02)

Reaction of bis(dichlorophenylstannyl)propane (PhCl2Sn)2(CH2)3 with Na2S gives the dimeric compound 2 (1) which has been shown by X-ray crystallography to contain six-membered SnC3SnS rings as well as eight-membered Sn4S4 rings.NMR studies

Transfer off hydrogen from carbon-hydrogen bonds. Synthesis, structure, and reactions of tris[(triphenylstannyl)methyl]methane

Ducharme, Yves,Latour, Stephan,Wuest, James D.

, p. 208 - 211 (2008/10/08)

Compounds in which a carbon-hydrogen bond is adjacent to several carbon-metal bonds promise to be particularly good donors of hydrogen. The synthesis, structure, and redox reactions of one member of this group of compounds, tris[(triphenylstannyl)methyl]methane (2), are reported. Triphenylcarbenium is reduced to triphenylmethane less rapidly by stannane 2 than by bis[(triphenylstannyl)methyl]methane (11). The unexpectedly low reactivity of stannane 2 is due to the adoption of a C3 conformation in which the central carbon-hydrogen bond is sterically shielded and gauche to the adjacent carbon-tin bonds.

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