![]() Dichloro(dimethylamino)phosphine structure
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Common Name | Dichloro(dimethylamino)phosphine | ||
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CAS Number | 683-85-2 | Molecular Weight | 145.95600 | |
Density | 1.271 g/mL at 25 °C(lit.) | Boiling Point | 150 °C(lit.) | |
Molecular Formula | C2H6Cl2NP | Melting Point | N/A | |
MSDS | Chinese USA | Flash Point | −10 °F | |
Symbol |
![]() ![]() GHS02, GHS05 |
Signal Word | Danger |
Synthesis and biological evaluation of fluorinated deoxynucleotide analogs based on bis-(difluoromethylene)triphosphoric acid.
Proc. Natl. Acad. Sci. U. S. A. 107(36) , 15693-15698, (2010) It is difficult to overestimate the importance of nucleoside triphosphates in cellular chemistry: They are the building blocks for DNA and RNA and important sources of energy. Modifications of biologically important organic molecules with fluorine are of grea... |
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Equilibrium conformation of dimethylaminodichlorophosphine molecule: the use of the results of quantum-chemical calculations and spectroscopic measurements in the analysis of gas-phase electron diffraction data. Khaikin LS, et al.
Russ. Chem. Bull. 50(9) , 1550-1562, (2001)
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Dimethylaminodimethylphosphine1. Burg AB and Slota Jr PJ.
J. Am. Chem. Soc. 80(5) , 1107-1109, (1958)
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35Cl NQR spectra of phosphorus chlorides and their molecular conformations in crystals. Part 1. Phosphorus (III) chlorides RPCl2. Kozlov ES, et al.
J. Mol. Struct. 550 , 167-175, (2000)
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Vibrational spectra and structure of dimethylaminodichlorophosphine. Durig JR and Casper JM
J. Phys. Chem. 75(25) , 3837-3843, (1971)
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Reactions of sulfur dioxide with aminophosphines. Light RW and Paine RT.
Phosph. Sulfur Relat. Elem. 8(3) , 255-258, (1980)
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Organophosphorus chemistry. Part XIV. Reaction of phosphorodiamidous chlorides with sulphonamides: a new route to diazadiphosphetidines. Bowden FL, et al.
J. Chem. Soc. Perkin Trans. I , 516-520, (1973)
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Reaction of 1, 1-dichloro-1-nitrosobutane with N, N-dimethylamidodichlorophosphite. Sokolov VB, et al.
Bull. Acad. Sci. USSR, Chemistry Series 38(6) , 1296-1298, (1989)
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