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595-90-4

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595-90-4 Usage

Chemical Properties

White powder. Insoluble in water; soluble in hot benzene, toluene, xylene.

Uses

Different sources of media describe the Uses of 595-90-4 differently. You can refer to the following data:
1. Stabilizer in chlorinated transformer oils, mothproofing agent, scavenger in dielectric fluids, intermediate.
2. Tetraphenyltin is used as stabilizer, catalyze, adhesion agent, it is used to produce other chemicals like, it can react with 3-chloro-2,5-diisobutyl-pyrazine to get 3,6-diisobutyl-2-phenylpyrazine. It is used as starting materials or catalysts.

Hazard

Skin irritant.

Purification Methods

It forms yellow crystals from CHCl3, pet ether (b 77-120o), xylene or *benzene/cyclohexane, and is dried at 75o/20mm. [Gilman & Rosenberg J Am Chem Soc 74 531 1952, Beilstein 16 IV 1592.]

Check Digit Verification of cas no

The CAS Registry Mumber 595-90-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,9 and 5 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 595-90:
(5*5)+(4*9)+(3*5)+(2*9)+(1*0)=94
94 % 10 = 4
So 595-90-4 is a valid CAS Registry Number.
InChI:InChI=1/4C6H5.Sn/c4*1-2-4-6-5-3-1;/h4*1-5H;/rC24H20Sn/c1-5-13-21(14-6-1)25(22-15-7-2-8-16-22,23-17-9-3-10-18-23)24-19-11-4-12-20-24/h1-20H

595-90-4 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (71117)  Tetraphenyltin   

  • 595-90-4

  • 100g

  • 664.0CNY

  • Detail
  • Alfa Aesar

  • (A19132)  Tetraphenyltin, 97%   

  • 595-90-4

  • 10g

  • 398.0CNY

  • Detail
  • Alfa Aesar

  • (A19132)  Tetraphenyltin, 97%   

  • 595-90-4

  • 250g

  • 974.0CNY

  • Detail
  • Alfa Aesar

  • (A19132)  Tetraphenyltin, 97%   

  • 595-90-4

  • 50g

  • 1082.0CNY

  • Detail
  • Aldrich

  • (T26727)  Tetraphenyltin  97%

  • 595-90-4

  • T26727-5G

  • 422.37CNY

  • Detail

595-90-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Tetraphenyltin

1.2 Other means of identification

Product number -
Other names Tetraphenylstannane

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:595-90-4 SDS

595-90-4Relevant articles and documents

Kupchik, E. J.,Connolly, R. E.

, p. 4747 - 4748 (1961)

Schwedt, G.,Ruessel, H. A.

, p. 301 - 303 (1973)

Coates, G. E.,Tranah, M.

, (1967)

-

Gilman,Rosenberg

, p. 2063 (1959)

-

Schmitz-Dumont

, p. 289,294 (1941)

The photochemistry of aromatic compounds IV. Photochemical behaviour of hexaphenylditin

Wilputte-Steinert,Nasielski

, p. 113 - 118 (1970)

The irradiation of hexaphenylditin yields "hot" triphenyltin radicals whose decomposition into diphenyltin and phenyl radicals competes with recombination and disproportionation.

The structures of ring-expanded NHC supported copper(

Charman, Rex S. C.,Liptrot, David J.,Lowe, John P.,Mahon, Mary F.

supporting information, p. 831 - 835 (2022/02/01)

Three ring-expanded N-heterocyclic carbene-supported copper(i) triphenylstannyls have been synthesised by the reaction of (RE-NHC)CuOtBu with triphenylstannane (RE-NHC = 6-Mes, 6-Dipp, 7-Dipp). The compounds were characterised by NMR spectroscopy and X-ray crystallography. Reaction of (6-Mes)CuSnPh3 with di-p-tolyl carbodiimide, phenyl isocyanate and phenylisothiocyanate gives access to a copper(i) benzamidinate, benzamide and benzothiamide respectively via phenyl transfer from the triphenylstannyl anion with concomitant formation of (Ph2Sn)n. Attempts to exploit this reactivity under a catalytic regime were hindered by rapid copper(i)-catalysed dismutation of Ph3SnH to Ph4Sn, various perphenylated tin oligomers, H2 and a metallic material thought to be Sn(0). Mechanistic insight was provided by reaction monitoring via NMR spectroscopy and mass spectrometry.

Continuous organomagnesium synthesis of organometallic compounds

Storozhenko,Grachev,Klochkov,Shiryaev

, p. 387 - 393 (2013/06/27)

Continuous organomagnesium synthesis of a number of organic derivatives of 14th group elements of the periodic table was examined in a column apparatus with an agitator. An effect of a molar ratio of reactants, temperature in a reaction zone, and other factors was studied on the yield and composition of the products.

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