4,4'-Bis(hydroxymethyl)-2,2'-bipyridine
4,4'-Bis(hydroxymethyl)-2,2'-bipyridine Basic information
- Product Name:
- 4,4'-Bis(hydroxymethyl)-2,2'-bipyridine
- Synonyms:
-
- [2-[4-(hydroxymethyl)-2-pyridinyl]-4-pyridinyl]methanol
- 2,2'-Bi(pyridine-4-methanol)
- 2,2'-Bipyridine-4,4'-bismethanol
- 2,2'-Bipyridine-4,4'-dimethanol
- {2-[4-(hydroxyMethyl)pyridin-2-yl]pyridin-4-yl}Methanol
- 4,4'-Bis(hydroxymethyl)-2,2'-bipyridine
- 2,2'-Bipyridine-4,4'-dimethanol 4,4'-Bis(hydroxymethyl)-2,2'-bipyridyl
- [2,2'-Bipyridine]-4,4'-diyldiMethanol
- CAS:
- 109073-77-0
- MF:
- C12H12N2O2
- MW:
- 216.24
- Product Categories:
-
- Pyridines derivates
- Mol File:
- 109073-77-0.mol
4,4'-Bis(hydroxymethyl)-2,2'-bipyridine Chemical Properties
- Melting point:
- 170.6-171.4 °C
- Boiling point:
- 450.4±40.0 °C(Predicted)
- Density
- 1.281±0.06 g/cm3(Predicted)
- storage temp.
- Keep in dark place,Sealed in dry,Room Temperature
- solubility
- soluble in Methanol
- form
- powder to crystal
- pka
- 12.94±0.10(Predicted)
- color
- White to Almost white
- InChI
- InChI=1S/C12H12N2O2/c15-7-9-1-3-13-11(5-9)12-6-10(8-16)2-4-14-12/h1-6,15-16H,7-8H2
- InChIKey
- RRXGRDMHWYLJSY-UHFFFAOYSA-N
- SMILES
- C1(C2=NC=CC(CO)=C2)=NC=CC(CO)=C1
Safety Information
- Safety Statements
- 24/25
- HS Code
- 29333990
4,4'-Bis(hydroxymethyl)-2,2'-bipyridine Usage And Synthesis
Uses
4,4‘-Bis(hydroxymethyl)-2,2’-bipyridine is a replication inhibitor that has been used in the treatment of cancer. It has also been shown to be effective in the treatment of metabolic disorders and chronic bronchitis.
Synthesis
1762-42-1
109073-77-0
The general procedure for the synthesis of 2,2'-bipyridine-4,4'-dimethanol from diethyl [2,2'-bipyridine]-4,4'-dicarboxylate was as follows: sodium borohydride (1.87 g, 49 mmol) was added to diethyl [2,2'-bipyridine]-4,4'-dicarboxylate (567 mg) dissolved in anhydrous ethanol (34 mL) , 1.89 mmol) suspension. The reaction mixture was refluxed for 3 hours. After completion of the reaction, it was cooled to room temperature and saturated ammonium chloride solution (24 mL/g NH4Cl) was added to quench the excess sodium borohydride. Subsequently, ethanol was removed by evaporation under reduced pressure. The resulting solid was dissolved in a minimal amount of water using an ultrasonic bath. The aqueous phase was extracted with ethyl acetate (5 x 34 mL) and the organic phases were combined and dried over anhydrous sodium sulfate. Finally, the organic phase was concentrated under reduced pressure to give a white powdery product in 91% yield.
References
[1] Chemical Communications, 2009, # 48, p. 7545 - 7547
[2] Electrochimica Acta, 2016, vol. 207, p. 313 - 320
[3] Journal of Physical Chemistry B, 1999, vol. 103, # 38, p. 8067 - 8079
[4] Patent: CN105793241, 2016, A. Location in patent: Paragraph 0129; 0159
[5] Tetrahedron, 2014, vol. 70, # 36, p. 6271 - 6275
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4,4'-Bis(hydroxymethyl)-2,2'-bipyridine(109073-77-0)Related Product Information
- 2,6-Lutidine
- 4,4'-Bipyridine
- Tris(hydroxymethyl)nitromethane
- DIPIPERIDINOMETHANE
- 2,2'-Bipyridine
- 2-(Hydroxymethyl)pyridine
- 2,5-PYRIDINEDICARBOXYLIC ACID
- Diethyl 1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylate
- 2,2'-Bipyridine-4,4'-dicarboxylic acid
- DIBUTYL 2,2'-BIPYRIDINE-4,4'-DICARBOXYLATE
- CIS-BIS(ISOTHIOCYANATO)BIS(2,2-BIPYRIDYL-4,4-DICARBOXYLATO)-RUTHENIUM(II)
- 2,2'-BIQUINOLINE-4,4'-DICARBOXYLIC ACID DIPOTASSIUM SALT TRIHYDRATE
- Bicinchoninic Acid Disodium Salt
- 2,2'-Bicinchoninic Acid
- 4,4'-Bis(ethoxycarbonly)-2,2'-bipyridine
- 4,4'-Bis(methoxycarbonly)-2,2'-bipyridine
- 2,2':6',2''-TERPYRIDINE-4,4',4''-TRICARBOXYLIC ACID
- Hydroxymethyl