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3,5-Dimethyl-4-methoxy-2-pyridinemethanol

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3,5-Dimethyl-4-methoxy-2-pyridinemethanol Basic information

Product Name:
3,5-Dimethyl-4-methoxy-2-pyridinemethanol
Synonyms:
  • ((4-Methoxy-3,5-dimethyl)-2-pyridinyl)methanol
  • 4-methoxy-3,5-dimethyl-2-pyridylmethanol
  • 2-HYDROXYMETHYL-4-METHOXY-3,5-DIMETHYLPYRIDINE
  • 2-HYDROXYMETHYL-3,5-DIMETHYL-4-METHOXY PYRIDINE
  • 3,5-DIMETHYL-2-HYDROXYMETHYL-4-METHOXYPYRIDINE
  • 3,5-DIMETHYL-4-METHOXY-2-PYRIDINE METHANOL
  • 4-METHOXY-3,5-DIMETHYL-2-HYDROXYMETHYL PYRIDINE
  • 4-METHOXY-3,5-DIMETHYL-2-PYRIDINEMETHANOL
CAS:
86604-78-6
MF:
C9H13NO2
MW:
167.21
EINECS:
289-258-5
Product Categories:
  • Heterocycle-Pyridine series
  • OLED materials,pharm chemical,electronic
  • Pharmaceutical intermediates
  • C9 to C46
  • Heterocyclic Building Blocks
  • Pyridines
  • Aromatic alcohols and diols
  • Pyridines derivates
  • bc0001
Mol File:
86604-78-6.mol
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3,5-Dimethyl-4-methoxy-2-pyridinemethanol Chemical Properties

Melting point:
56.5-60.5 °C(lit.)
Boiling point:
115-135 °C(Press: 0.01 Torr)
Density 
1.092±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Room Temperature
solubility 
Chloroform (Slightly)
form 
Solid
pka
13.27±0.10(Predicted)
color 
Off-White
InChI
InChI=1S/C9H13NO2/c1-6-4-10-8(5-11)7(2)9(6)12-3/h4,11H,5H2,1-3H3
InChIKey
PSEPRWKZZJWRCB-UHFFFAOYSA-N
SMILES
C1(CO)=NC=C(C)C(OC)=C1C
CAS DataBase Reference
86604-78-6(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
HS Code 
29333990

MSDS

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3,5-Dimethyl-4-methoxy-2-pyridinemethanol Usage And Synthesis

Chemical Properties

White to light brown powder or crystal

Uses

(4-Methoxy-3,5-dimethylpyridin-2-yl)methanol can be used as wear-resistant rubber.

General Description

4-Methoxy-3,5-dimethyl-2-pyridinemethanol is a pyridine derivative.

Synthesis

86604-75-3

86604-78-6

General procedure for the synthesis of 4-methoxy-3,5-dimethyl-2-hydroxymethylpyridine from 2-chloromethyl-3,5-dimethyl-4-methoxypyridine hydrochloride: 80 g of 2-chloromethyl-4-methoxy-3,5-dimethylpyridine hydrochloride was taken and 300 ml of methanol and 150 ml of water were added followed by 5.4 g of potassium iodide and 40.4 g of sodium hydroxide. The mixture was stirred and heated to reflux and the reaction lasted for 4 hours. Upon completion of the reaction, the methanol was removed by rotary evaporator. To the residue, 300 ml of drinking water was added, followed by extraction with dichloromethane (150 ml each time, 3 times). The organic phases were combined, washed with saturated sodium chloride solution and dried with anhydrous sodium sulfate. Finally, the organic phase was concentrated to give 50.0 g of a red oily liquid in 83.0% yield.

References

[1] Patent: CN107382963, 2017, A. Location in patent: Paragraph 0013; 0017; 0021

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