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3910-39-2

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3910-39-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3910-39-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,1 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3910-39:
(6*3)+(5*9)+(4*1)+(3*0)+(2*3)+(1*9)=82
82 % 10 = 2
So 3910-39-2 is a valid CAS Registry Number.
InChI:InChI=1/3C6F5.Sb/c3*7-2-1-3(8)5(10)6(11)4(2)9;/rC18F15Sb/c19-1-4(22)10(28)16(11(29)5(1)23)34(17-12(30)6(24)2(20)7(25)13(17)31)18-14(32)8(26)3(21)9(27)15(18)33

3910-39-2Relevant articles and documents

Catalysis with Pnictogen, Chalcogen, and Halogen Bonds

Benz, Sebastian,Poblador-Bahamonde, Amalia I.,Low-Ders, Nicolas,Matile, Stefan

supporting information, p. 5408 - 5412 (2018/03/23)

Halogen- and chalcogen-based σ-hole interactions have recently received increased interest in non-covalent organocatalysis. However, the closely related pnictogen bonds have been neglected. In this study, we introduce conceptually simple, neutral, and mon

TRIORGANOANTIMONY COMPOUNDS FOR PESTICIDAL USE

-

Page/Page column 15-16; 23; 24, (2008/06/13)

The invention concerns with synthesis of mixed triorganoantimony (III) compounds bearing halophenyl groups ("R2SbR1") , using metal turnings viz Lithium, Magnesium or Zinc in donor solvents with plurality of uses as microbiocides and insecticides for cont

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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