|O|-(2-Oxo-1(2H)pyridyl)-|N|,|N|,|N|',|N|'-tetramethyluronium tetrafluoroborate

Suppliers

Names

[ Name ]:
|O|-(2-Oxo-1(2H)pyridyl)-|N|,|N|,|N|',|N|'-tetramethyluronium tetrafluoroborate

[Synonym ]:
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

Chemical & Physical Properties

[ Melting Point ]:
140 °C (dec.)(lit.)

[ 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

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ 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

Customs

[ HS Code ]: 2933399090

[ 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%

Articles

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)...

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...

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...

4-((Cyclohexylamino)methyl)benzoic acid hydrochloride
1-[(2,4-Dichlorophenyl)methyl]-N-(1,1-dimethylethyl)-2-methyl-1H-indole-3-methanamine
2-Methoxy-6-(pyrazol-1-yl)-benzonitrile
1H-3-Benzazepin-7-ol, 8-chloro-2,3,4,5-tetrahydro-5-(3-iodophenyl)-3-methyl-, (S)-
(4-Methyl-tetrahydro-furan-2-yl)-methanol
N-(1-cyanocyclopentyl)-2-[4-(4-fluorobenzenesulfonyl)-1,4-diazepan-1-yl]acetamide
4,5,6,7-Tetrahydrobenzo[d]isoxazole-3-carbaldehyde
tert-Butyl-DL-alanine
4-amino-N-[2-tert-butyl-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-benzimidazol-5-yl]-N-ethylbenzenesulfonamide
N-[3-(Aminooxy)propyl]-N-butyl-1-butanamine