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Difluoro(diphenyl)stannane, also known as diphenyltin difluoride, is an organotin compound with the chemical formula (C6H5)2SnF2. It is a colorless, crystalline solid that is sensitive to air and moisture. difluoro(diphenyl)stannane is primarily used as a catalyst in various organic reactions, such as the hydrostannation of alkenes and alkynes, as well as in the synthesis of other organotin compounds. Difluoro(diphenyl)stannane is also employed in the production of certain polymers and as a precursor in the preparation of other organotin derivatives. Due to its reactivity and potential toxicity, it is essential to handle this chemical with care and in accordance with proper safety protocols.

312-41-4

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312-41-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 312-41-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,1 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 312-41:
(5*3)+(4*1)+(3*2)+(2*4)+(1*1)=34
34 % 10 = 4
So 312-41-4 is a valid CAS Registry Number.

312-41-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Stannane, difluorodiphenyl-

1.2 Other means of identification

Product number -
Other names diphenylvinylphosphine sulphide

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:312-41-4 SDS

312-41-4Downstream Products

312-41-4Relevant academic research and scientific papers

Synthesis, Reactivity and Spectral Studies of Some Pentacoordinate Tin(IV) Complexes Derived from Triphenyltin Trifluoroacetate

Srivastava, T. N.,Singh, Jai Deo

, p. 489 - 492 (2007/10/02)

Triphenyltin methoxide/ethoxide prepared in situ reacts with trifluoroacetic acid, yielding triphenyltin trifluoroacetate in quantitative yield.The reactions of Ph3SnOCOCF3 with tetraalkylammonium salts (R4NX) give pentacoordinated Sn(IV) complex anions of the general formulae (+)(-) .Ph3SnOCOCF3 undergoes cleavage with electrophilic reagents such as ICl, IBr, HgCl2, Hg(SCN)2, yielding Ph2Sn(OCOCF3)*X (X=Cl, Br, SCN).These compounds like the parent Ph3SnOCOCF3 are polymeric in nature with five coordinated Sn(IV) atoms and bridging trifluoroacetate groups.These undergo nucleophilic substitution of (X) with other electronegative groups and form 1:1 molecular adducts with common Lewis bases.All these compounds have been characterized by elemental analyses, and IR and PMR data.

THE SYNTHESIS AND TIN-119m MOESSBAUER SPECTRA OF SOME DIORGANOTIN DIHALIDE AND DIPSEUDOHALIDE COMPLEXES WITH NITROGEN AND OXYGEN-DONOR LIGANDS

Crowe, Alan J.,Smith, Peter J.

, p. 223 - 236 (2007/10/02)

The synthesis and 119mSn Moessbauer spectra of 114 complexes of the type R2SnX2, L2 (R = Me, Et, n-Pr, n-Bu, n-Oct, Ph, Bz; X = F, Cl, Br, I, NCS; L2 = 2 monodentate or 1 bidentate O- or N-donor ligand(s)), 74 of which are new, are reported.The majority of the complexes are isostructural, having an octahedral trans-R2SnX4 geometry about tin, whilst five of the diphenyltin complexes (R = Ph; X = Cl; L2 = AMP, Nphen; X = NCS; L2 = bipy, phen, TMphen) adopt a cis-R2SnX4 octahedral structure.A convenient method for the synthesis of a number of novel 1:1 diorganotin difluoride complexes using hot acetonitrile is reported and a structure for the unusual adduct, Ph2SnF2 * 0.5 phen, is proposed.

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