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Tris(2-methylphenyl)tin, also known as triphenyltin (TPT), is an organotin compound with the chemical formula (C6H5CH3)3Sn. It is a colorless, crystalline solid that is insoluble in water but soluble in organic solvents. TPT has been widely used as a fungicide in agriculture, particularly for the control of various plant diseases caused by fungi, such as powdery mildew and rust. It is also used as a wood preservative and an antifouling agent in marine paints. However, due to its potential environmental and health risks, including endocrine disruption and bioaccumulation in aquatic organisms, the use of TPT has been restricted or banned in many countries.

83183-32-8

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83183-32-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83183-32-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,1,8 and 3 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 83183-32:
(7*8)+(6*3)+(5*1)+(4*8)+(3*3)+(2*3)+(1*2)=128
128 % 10 = 8
So 83183-32-8 is a valid CAS Registry Number.

83183-32-8Downstream Products

83183-32-8Relevant academic research and scientific papers

Ueber gemischte Gruppe 14-Gruppe 14-Bindungen. VI. Hexa-o-tolylethan-Analoga o-Tol6Sn2, o-Tol6PbSn und o-Tol6Pb2: ein Vergleich von Bindungsstaerke und Polaritaet in der Reihung Sn-Sn, Pb-Sn, Pb-Pb

Schneider-Koglin, Claudia,Behrends, Kerstin,Draeger, Martin

, p. 29 - 38 (2007/10/02)

The lead-tin compounds o-Tol6PbSn, o-Tol3PbSnPh3 and Mes3PbSnPh3 have been synthesized from Li and halide precursors in THF/ether at low temperatures.The crystal structures of the S4 symmetric o-Tol4Pb and of the three isomorphous title compounds have bee

Sterically Hindered Free Radicals, IX. Generation and Structure of Stannyl Radicals R3Sn* with Bulky Groups

El-Farargy, Ahmed F.,Lehnig, Manfred,Neumann, Wilhelm P.

, p. 2783 - 2794 (2007/10/02)

Methylated phenyl groups in hexaaryldistannanes cause reversible thermal dissociation R3Sn-SnR3 (1) 2 R3Sn* (2) only if at least the 2,6-positions are methylated.Further methyl groups enhance this dissociation only when neighbouring these positions and each other, thus causing a buttressing effect .So, DSn-Sn is decreased (51.5 -> 38.5 kcal/mol).ESR data and geometry of 2 are reported, as well as those of stannyl radicals 2, R = PhmMenCCH2 (m + n = 3) generated from the corresponding hydrides.The rotation around C-Sn bonds is hindered with increasing m.A preferred conformation is concluded from ESR data.Numerous compounds 1, R3SnH, and other precursors are prepared for the first time.

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