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Sulfanide, also known as sodium sulfide, is a chemical compound with the formula Na2S. It is a strong reducing agent and is used in various applications such as water treatment, leather processing, and as a reagent in chemical analysis. Triphenyllead, on the other hand, is an organolead compound with the formula (C6H5)3Pb. It is a colorless, crystalline solid that is sensitive to light and air, and is used as a catalyst in organic synthesis and as a stabilizer in PVC plastics. Both sulfanide and triphenyllead have distinct properties and applications, with sulfanide being a strong reducing agent and triphenyllead being a versatile organometallic compound.

1802-88-6

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1802-88-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1802-88-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,0 and 2 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1802-88:
(6*1)+(5*8)+(4*0)+(3*2)+(2*8)+(1*8)=76
76 % 10 = 6
So 1802-88-6 is a valid CAS Registry Number.

1802-88-6Downstream Products

1802-88-6Relevant academic research and scientific papers

Structural studies on Ph3MSMPh3 (M = Sn, Pb): Quest for a metal-metal bond

Singh, Neetu,Prasad, Rajendra,Bhattacharya, Subrato

, p. 548 - 552 (2009)

The title compounds Ph3PbSPbPh3 (1) and Ph3SnSSnPh3 (2) were prepared in high yields by a reaction of Na2S, respectively, with Ph3Pb(SOCMe) and Ph3Sn(SOCMe). X-ray crystallograph

19F NMR studies of the comparative electronegativity of the Ph3E groups (E = C, Si, Ge, Sn, or Pb) in Ph3E derivatives of tris(4-fluorophenyl)stannanethiol

Kravtsov,Peregudov,Krylova,Gorelikova

, p. 1167 - 1170 (2007/10/03)

Compounds (4-FC6H4)3SnSEPh3 (E = C, Si, Ge, Sn, or Pb) were synthesized or generated in solution. The data on the comparative electronegativity of the Ph3E groups were obtained from the results of su

Synthesis and some reactions of tris (pentafluorophenyl) antimony compounds

Raj, Prem,Saxena,Singhal, Kiran,Ranjan, Ashok

, p. 251 - 258 (2008/10/08)

(C6F5)3Sb has been found to react with interhalogens and halo-pseudohalogens, IX(X = Cl, Br, N3 and NCO), pseudohalogen (SCN), and elemental sulphur to give oxidative addition products (I-VI). (C6F5)3SbS(VI) may also be prepared by the reaction of (C6F5)3SbCl2 with H2S. Metathetical reactions of (C6F5)3SbCl2 with appropriate metallic salts yield covalent pentacoordinate disubstituted products (V, VII-XII) of the general formula, (C6F5)3SbY2 (Y = NCS, NCO, -ONCMe2, -ONCMePh -NCO(CH2)2CO and p-NO2C6H4OCO). Treatment of (C6F5)3SbCl2 with aqueous NaN3 gives the binuclear oxo-bridge compound, [(C6F5)3SbOSb(C6F5)3](N3)2·(III) and (IV) are also accessible by displacement reaction of (I) or (II) with the corresponding metallic salt. Molecular weight, conductance measurements, and IR spectra on the new organoantimony(V) derivatives have been obtained. Reductive cleavage reactions of (C6F5)3SbS with hexaaryldileads, Ar6Pb2(Ar = Phenyl, p-tolyl) produce (C6F5)3Sb and the corresponding bis(triaryllead) sulphide but treatment of (C6F5)3SbX2(X = NCO, Cl) with Ar6Pb2 gave Ar4Pb and Ar2PbX2 together with (C6F5)3Sb. (C6F5)3SbCl2 and bis(triorganotin)sulphides undergo exchange of anionic groups.

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