diallyl n,n-diisopropylphosphoramidite
diallyl n,n-diisopropylphosphoramidite structure
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Common Name | diallyl n,n-diisopropylphosphoramidite | ||
|---|---|---|---|---|
| CAS Number | 126429-21-8 | Molecular Weight | 245.29800 | |
| Density | 0.928 g/mL at 25 °C(lit.) | Boiling Point | 220.8ºC at 760mmHg | |
| Molecular Formula | C12H24NO2P | Melting Point | N/A | |
| MSDS | Chinese USA | Flash Point | 87.4ºC | |
| Symbol |
GHS02, GHS07 |
Signal Word | Warning | |
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A highly convergent synthesis of myristoyl-carba(dethia)-coenzyme A.
European J. Org. Chem. 2010(9) , 1728-1735, (2010) Co-translational myristoylation of the N-terminal glycine residue of diverse signaling proteins is required for membrane attachment and proper function of these molecules. The transfer of myristate from myristoyl-coenzyme A (myr-CoA) is catalyzed by the enzym... |
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Red-emitting rhodamines with hydroxylated, sulfonated, and phosphorylated dye residues and their use in fluorescence nanoscopy.
Chemistry 18(41) , 12986-98, (2012) Fluorescent dyes emitting red light are frequently used in conventional and super-resolution microscopy of biological samples, although the variety of the useful dyes is limited. We describe the synthesis of rhodamine-based fluorescent dyes with absorption an... |
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Solid-phase synthesis of adenosine phosphopeptides as potential bisubstrate inhibitors of protein kinases. Medzihradszky D, et al.
J. Am. Chem. Soc. 116(21) , 9413-19, (1994)
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