2-Phenylacetic dithioperoxyanhydride
2-Phenylacetic dithioperoxyanhydride structure
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Common Name | 2-Phenylacetic dithioperoxyanhydride | ||
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| CAS Number | 15088-78-5 | Molecular Weight | 302.411 | |
| Density | 1.3±0.1 g/cm3 | Boiling Point | 481.1±48.0 °C at 760 mmHg | |
| Molecular Formula | C16H14O2S2 | Melting Point | 59-63 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 210.1±19.6 °C | |
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Synthesis and biological activity of PTEN-resistant analogues of phosphatidylinositol 3,4,5-trisphosphate.
J. Am. Chem. Soc. 128(51) , 16464-5, (2006) The activation of phosphatidylinositol 3-kinase (PI 3-K) and subsequent production of PtdIns(3,4,5)P3 launches a signal transduction cascade that impinges on a plethora of downstream effects on cell physiology. Control of PI 3-K and PtdIns(3,4,5)P3 levels is ... |
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Synthesis of antisense oligonucleotides: Replacement of 3H-1, 2-benzodithiol-3-one 1, 1-dioxide (Beaucage reagent) with phenylacetyl disulfide (PADS) as efficient sulfurization reagent: From bench to bulk manufacture of active pharmaceutical ingredient. Cheruvallath ZS, et al.
Org. Process Res. Dev. 4(3) , 199-204, (2000)
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Use of phenylacetyl disulfide (PADS) in the synthesis of oligodeoxyribonucleotide phosphorothioates. Cheruvallath ZS, et al.
Nucleosides Nucleotides Nucleic Acids 18(3) , 485-492, (1999)
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A study on the use of phenylacetyl disulfide in the solid-phase synthesis of oligodeoxynucleoside phosphorothioates. Roelen HCPF, et al.
J. R. Neth. Chem. Soc. 110(7-8) , 325-331, (1991)
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