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Tributylstannanecarbonitrile | CAS:2179-92-2
Tributylstannanecarbonitrile
  • Name:Tributylstannanecarbonitrile
  • CAS:2179-92-2
  • Synonyms:Tributylstannyl cyanide; Tributyltin cyanide; Cyanotributyltin; Tributylcyanostannane
  • Molecular Formula:C13H27NSn
  • Molecular Weight:316.07
  • EINESC:

Description

Properties

Melting point 93.0-96.5 ºC (acetonitrile

Safety

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SDS

Source SDS/MSDS Samples
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Articles
Peer-Reviewed Papers
Calculations of the energy distribution from perturbation peak data--a new tool for characterization of chromatographic phases.Jörgen Samuelsson et al.Journal of chromatography. A, 1203(2), 177-184 (2008-08-02) Screening and immobilization Burkholderia sp. GXU56 lipase for enantioselective resolution of (R,S)-methyl mandelate.Han-Ning Wei et al.Applied biochemistry and biotechnology, 149(1), 79-88 (2008-03-20) Integration of newly isolated biocatalyst and resin-based in situ product removal technique for the asymmetric synthesis of (R)-methyl mandelate.Jin-Ling Guo et al.Bioprocess and biosystems engineering, 33(7), 797-804 (2009-12-25) Esters of mandelic acid as substrates for (S)-mandelate dehydrogenase from Pseudomonas putida: implications for the reaction mechanism.Asteriani R Dewanti et al.Biochemistry, 43(7), 1883-1890 (2004-02-18) Enantiomer separation of mandelates and their analogs on cyclodextrin derivative chiral stationary phases by capillary GC.M Y Nie et al.Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 17(10), 1183-1187 (2002-05-07) Hydrolysis of triacetin catalyzed by immobilized lipases: effect of the immobilization protocol and experimental conditions on diacetin yield.Karel Hernandez et al.Enzyme and microbial technology, 48(6-7), 510-517 (2011-11-25) Compensation of the enantioselectivity-activity trade-off in the directed evolution of an esterase from Rhodobacter sphaeroides by site-directed saturation mutagenesis.Fei Guo et al.Applied microbiology and biotechnology, 97(8), 3355-3362 (2012-11-28) Generation of the enol of methyl mandelate by flash photolysis of methyl phenyldiazoacetate in aqueous solution and study of rates of ketonization of this enol in that medium.Y Chiang et al.The Journal of organic chemistry, 65(4), 1175-1180 (2000-05-18) Theoretical study on chiral recognition mechanism of methyl mandelate enantiomers on permethylated β-cyclodextrin.Jie-Hua Shi et al.Journal of molecular modeling, 18(2), 803-813 (2011-05-20)
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