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194800-56-1

194800-56-1 Structure

194800-56-1 Structure
IdentificationBack Directory
[Name]

4,4'-BIS(DIHYDROXYPHOSPHORYL)-2,2'-BIPYRIDINE
[CAS]

194800-56-1
[Synonyms]

4,4'-diphosphonic acid-2,2'-bipyridine
2,2'-Bipyridine-4,4'-diphosphonic Acid
[2,2'-Bipyridine]-4,4'-diyldiphosphonic acid
4,4'-BIS(DIHYDROXYPHOSPHORYL)-2,2'-BIPYRIDINE
2,2'-Bipyridine-4,4'-bis(phosphonic acid) 97%
2,2'-bipyridine-4,4'-diylbis(phosphonic acid)
Phosphonic acid, P,P'-[[2,2'-bipyridine]-4,4'-diyl]bis-
[2-(4-phosphonopyridin-2-yl)pyridin-4-yl]phosphonic acid
[Molecular Formula]

C10H10N2O10P2
[MDL Number]

MFCD11042490
[MOL File]

194800-56-1.mol
[Molecular Weight]

316.14
Chemical PropertiesBack Directory
[Boiling point ]

741.1±70.0 °C(Predicted)
[density ]

1.78±0.1 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,Room Temperature
[pka]

0.06±0.10(Predicted)
[Appearance]

Off-white to light yellow Solid
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

4,4'-BIS(DIHYDROXYPHOSPHORYL)-2,2'-BIPYRIDINE(194800-56-1)1HNMR
Hazard InformationBack Directory
[Synthesis]

TETRAETHYL 2,2'-BIPYRIDINE-4,4'-BISPHOSPHONATE

174397-53-6

4,4'-BIS(DIHYDROXYPHOSPHORYL)-2,2'-BIPYRIDINE

194800-56-1

Diethyl 2,2'-bipyridine-4,4'-bisphosphonate (1.26 g, 2.94 mmol, 1.00 eq.) was dissolved in anhydrous dichloromethane under argon protection. To this solution was added bromotrimethylsilane (4.50 g, 29.4 mmol, 10.0 eq.), and the resulting yellow solution was stirred and reacted at room temperature for 24 hours. Upon completion of the reaction, methanol was slowly added dropwise until the color of the reaction mixture changed from yellow to colorless. Subsequently, extraction was carried out with water and 2,2'-bipyridine-4,4'-bisphosphonic acid (Compound 7) was isolated as a light yellow solid (0.93 g, 4.49 mmol, quantitative yield). The structure of the product was confirmed by nuclear magnetic resonance hydrogen (1H NMR, 400 MHz, DMSO-d6) and phosphorus spectra (31P NMR, 500 MHz, CDCl3): 1H NMR δ 8.85 (t, J = 4.5 Hz, 2H), 8.67 (d, J = 13.6 Hz, 2H), 7.73 (dd, J = 12.4, 4.8 Hz, 2H); 31P NMR δ 8.45 (s).

[References]

[1] Dyes and Pigments, 2014, vol. 104, p. 24 - 33
[2] Tetrahedron Letters, 1998, vol. 39, # 22, p. 3689 - 3692
[3] Inorganic Chemistry, 2015, vol. 54, # 2, p. 460 - 469
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