Cas no 1089-59-4 (Stannane,methyltriphenyl-)
Stannane,methyltriphenyl- structure
Product Name:Stannane,methyltriphenyl-
CAS No:1089-59-4
MF:C19H18Sn
MW:365.056224346161
CID:142385
PubChem ID:136855
Update Time:2025-04-19
Stannane,methyltriphenyl- Chemical and Physical Properties
Names and Identifiers
-
- Stannane,methyltriphenyl-
- methyl(triphenyl)stannane
- Methyltriphenyltin
- AC1L39FE
- methyl(triphenyl)tin
- Methyltriphenylstananne
- Methyltriphenylstannane
- methyltriphenyltin(IV)
- Methyltriphenyltin1000μg
- NSC179744
- Tin, methyltriphenyl-
- triphenylmethylstannane
- triphenylmetylstannane
- triphenyltin(IV) chloride
- NSC-179744
- NSC 179744
- Stannane, methyltriphenyl-
- 1089-59-4
- DTXSID30148767
-
- Inchi： 1S/3C6H5.CH3.Sn/c3*1-2-4-6-5-3-1;;/h3*1-5H;1H3;
- InChI Key： HMFXHBPQJQEFJF-UHFFFAOYSA-N
- SMILES： [Sn](C)(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1
Computed Properties
- Exact Mass: 358.04594
- Monoisotopic Mass: 366.043053g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 0
- Heavy Atom Count: 20
- Rotatable Bond Count: 3
- Complexity: 235
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 0?2
Experimental Properties
- PSA: 0
Stannane,methyltriphenyl- Related Literature
-
1. Synthesis of chiral organotin reagents: synthesis of enantiomerically enriched bicyclo[2.2.1]hept-2-yl tin hydrides from camphor. X-Ray crystal structures of (dimethyl)[(1R,2S,4R)-1,7,7-trimethylbicyclo[2.2.1]hept-2-yl]tin chloride and methyl(phenyl)bis[(1R,2S,4R)-1,7,7-trimethylbicyclo[2.2.1]hept-2-yl]stannaneMadeleine Helliwell,Eric J. Thomas,Linda A. Townsend J. Chem. Soc. Perkin Trans. 1 2002 1286
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2. Synthesis of chiral organotin reagents: synthesis of bicyclo[2.2.1]heptan-2-yl(diphenyl)tin hydrides with cis-disposed, oxygen-containing substituentsRobert M. Pratt,Eric J. Thomas J. Chem. Soc. Perkin Trans. 1 1998 727
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3. 286. Addition compounds of organotin halides with Lewis basesI. R. Beattie,G. P. McQuillan J. Chem. Soc. 1963 1519
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4. Intermolecular exchange and configurational stability of organotin alkoxides and phenoxidesUgo Folli,Dario Iarossi,Ferdinando Taddei J. Chem. Soc. Perkin Trans. 2 1973 1284
-
5. 1H nuclear magnetic resonance study of (d–p)π interactions in stannanes containing unsaturated systemsG. Barbieri,F. Taddei J. Chem. Soc. Perkin Trans. 2 1972 1323
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