|O|-(2-Oxo-1(2H)pyridyl)-|N|,|N|,|N|',|N|'-tetramethyluronium tetrafluoroborate structure
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Common Name | |O|-(2-Oxo-1(2H)pyridyl)-|N|,|N|,|N|',|N|'-tetramethyluronium tetrafluoroborate | ||
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CAS Number | 125700-71-2 | Molecular Weight | 297.058 | |
Density | N/A | Boiling Point | N/A | |
Molecular Formula | C10H16BF4N3O2 | Melting Point | 140 °C (dec.)(lit.) | |
MSDS | Chinese USA | Flash Point | N/A |
Name | 2-(2-Pyridon-1-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate |
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Synonym | More Synonyms |
Melting Point | 140 °C (dec.)(lit.) |
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Molecular Formula | C10H16BF4N3O2 |
Molecular Weight | 297.058 |
Exact Mass | 297.127167 |
PSA | 37.48000 |
LogP | 0.76660 |
Storage condition | 2-8°C |
Water Solubility | insoluble |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
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Hazard Codes | Xn:Harmful; |
Risk Phrases | R20/21/22;R36/37/38 |
Safety Phrases | S36/37/39-S26 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
HS Code | 2933399090 |
HS Code | 2933399090 |
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Summary | 2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
Rapid esterification of nucleosides to solid-phase supports for oligonucleotide synthesis using uronium and phosphonium coupling reagents.
Bioconjug. Chem. 10 , 1051-1057, (1999) Nucleosides can be esterified to solid-phase supports using uronium or phosphonium coupling reagents and a coupling additive, such as 1-hydroxybenzotriazole (HOBT), 7-aza-1-hydroxybenzotriazole (HOAT)... |
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Structural mimicry of the α-helix in aqueous solution with an isoatomic α/β/γ-peptide backbone.
J. Am. Chem. Soc. 133 , 7336-7339, (2011) Artificial mimicry of α-helices offers a basis for development of protein-protein interaction antagonists. Here we report a new type of unnatural peptidic backbone, containing α-, β-, and γ-amino acid... |
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Synthesis and biological evaluation of pyridin-2-one nucleosides.
Nucleosides Nucleotides 20 , 731-733, (2001) The synthesis of 1-(beta-D-ribofuranosyl)pyridin-2-one-3-carboxylic acid and the 3-carboxamide as well as a short series of 3N-carboxamides, prepared by TPTU/HOBt coupling of primary amines with 1-(be... |
O-(1,2-Dihydro-2-oxo-1-pyridyl)-N,N,N‘,N‘-tetramethyluronium tetrafluoroborate |
O-[2-Oxo-1(2H)-pyridyl]-N,N,N',N'-tetramethyluronium Tetrafluoroborate |
(Dimethylamino)-N,N-dimethyl[(2-oxo-1(2H)-pyridinyl)oxy]methaniminium tetrafluoroborate |
O-(1,2-dihydro-2-oxo-pyridyl)-1,1,3,3-tetramethyluronium tetrafluoroborate |
Bis(dimethylamino)[(2-oxopyridin-1(2H)-yl)oxy]methylium tetrafluoroborate |
O-(1,2-Dihydro-2-oxo-1-pyridyl)-N,N,N',N'-tetramethyluronium tetrafluoroborate |
MFCD00075475 |
[dimethylamino-(2-oxopyridin-1-yl)oxymethylidene]-dimethylazanium,tetrafluoroborate |
O-(2-Oxo-1(2H)Pyridyl)-N,N,N′,N′-Tetramethyluronium Tetrafluoroborate |
N-{(Dimethylamino)[(2-oxopyridin-1(2H)-yl)oxy]methylene}-N-methylmethanaminium tetrafluoroborate |
2-(2-Pyridon-1-yl)-1,1,3,3-tetram |
TPTU |