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

Modify Date: 2024-01-02 19:12:29

|O|-(2-Oxo-1(2H)pyridyl)-|N|,|N|,|N|',|N|'-tetramethyluronium tetrafluoroborate Structure
|O|-(2-Oxo-1(2H)pyridyl)-|N|,|N|,|N|',|N|'-tetramethyluronium tetrafluoroborate structure
Common Name |O|-(2-Oxo-1(2H)pyridyl)-|N|,|N|,|N|',|N|'-tetramethyluronium tetrafluoroborate
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

 Names

Name 2-(2-Pyridon-1-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate
Synonym More Synonyms

 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

 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%

 Articles4

More 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...

 Synonyms

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
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