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Stannane, [(2-methoxybenzoyl)oxy]triphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

91266-58-9

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91266-58-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91266-58-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,2,6 and 6 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 91266-58:
(7*9)+(6*1)+(5*2)+(4*6)+(3*6)+(2*5)+(1*8)=139
139 % 10 = 9
So 91266-58-9 is a valid CAS Registry Number.

91266-58-9Downstream Products

91266-58-9Relevant academic research and scientific papers

Organo-tin compounds having anti-tumour activity and anti-tumour compositions

-

, (2008/06/13)

The invention relates to anti-tumor compositions containing as an active ingredient one or more compounds of the formula wherein X and Y are each H, OH, halogen or alkyl; and Z is halogen, amino, alkoxy, acyloxy, sulphonic acid or alkyl. A number of these compounds are novel compounds.

Organotin Biocides. Part 11. Triphenyltin Benzoates: Electronic versus Steric Control of Structure

Molloy, Kieran C.,Blunden, Stephen J.,Hill, Robin

, p. 1259 - 1266 (2007/10/02)

Twenty four triphenyltin derivatives of substituted benzoic acids have been synthesised.On the basis of i.r., (119)Sn n.m.r. and Moessbauer spectroscopic data, structures have been assigned to these compounds as either tetrahedral monomers or trans-SnR3O2

Intramolecularly formed pentacoordinated structures of triphenyltin esters of salicylic acid, o-anisic acid, and p-methylthiobenzoic acid

Vollano, Jean F.,Day, Roberta O.,Rau, Denise N.,Chandrasekhar,Holmes, Robert R.

, p. 3153 - 3160 (2008/10/08)

Triphenyltin esters were formed by the reaction of bis(triphenyltin) oxide with salicylic acid, o-anisic acid, and p-methylthiobenzoic acid, 6-8, respectively. X-ray analysis revealed pentacoordinated structures containing Ph3Sn coordinated to the carboxylate group for 7 and 8. The structural distortion for each is a displacement from the tetrahedron toward a trigonal bipyramid. For 6, the structure contains an intramolecular oxygen atom interaction, in addition to hydrogen-bonding effects, with a resultant geometry close to tetrahedral. Infrared data confirm that carboxylate coordination occurs in solution. Factors influencing the appearance of the discrete five-coordinated form 6-8 relative to five-coordinated tin in a chain arrangement for related derivatives is discussed. For 6, the monoclinic space group P21/c (Z = 4) was obtained with a = 13.318 (6) ?, b = 12.113 (2) ?, c = 14.590 (4) ?, and β = 116.47 (3)°. Refinement gave R = 0.022 and Rw = 0.032. 7 crystallizes in the triclinic space group P1 (Z = 2) with a = 10.632 (2) ?, b = 11.452 (2) ?, c = 11.719 (2) ?, α = 62.86 (2)°, β = 71.95 (2)°, and γ = 62.31 (2)°. Refinement gave R = 0.024 and Rw = 0.041. For 8, the triclinic space group P1 resulted with a = 8.814 (1) ?, b = 9.816 (1) ?, c = 14.430 (3) ?, α = 89.39 (1)°, β = 80.19 (1)°, and γ = 68.89 (1)°. Refinement gave R = 0.025 and Rw = 0.040.

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