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(R)-(+)-1-(4-PYRIDYL)ETHANOL

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(R)-(+)-1-(4-PYRIDYL)ETHANOL Basic information

Product Name:
(R)-(+)-1-(4-PYRIDYL)ETHANOL
Synonyms:
  • 4-[(R)-1-Hydroxyethyl]pyridine
  • (R)-4-(1-Hydroxyethyl)pyridine,99+%,(99+% ee)
  • (R)-4-(1-Hydroxyethyl)pyridine(R)-(+)-1-(4-Pyridyl)ethanol
  • (R)-1-(pyridin-4-yl)ethanol
  • (1R)-1-(pyridin-4-yl)ethan-1-ol
  • 4-PyridineMethanol, α-Methyl-, (R)-
  • (aR)-a-Methyl-4-PyridineMethanol
  • (R)-(+)-alpha-Methyl-4-pyridinemethanol 99%
CAS:
27854-88-2
MF:
C7H9NO
MW:
123.15
Product Categories:
  • Alcohols, Hydroxy Esters and Derivatives
  • Chiral Compounds
Mol File:
27854-88-2.mol
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(R)-(+)-1-(4-PYRIDYL)ETHANOL Chemical Properties

Melting point:
67-69 °C(lit.)
Boiling point:
239.7±15.0 °C(Predicted)
Density 
1.082±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,2-8°C
solubility 
soluble in Methanol
pka
13.52±0.20(Predicted)
form 
Crystalline Powder or Needles
color 
White
optical activity
[α]20/D +55°, c = 1 in chloroform
BRN 
4306037
InChIKey
HVOAMIOKNARIMR-ZCFIWIBFSA-N
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
3-10
HS Code 
29333999

MSDS

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(R)-(+)-1-(4-PYRIDYL)ETHANOL Usage And Synthesis

Reaction

  1. Used for the synthesis of chiral 1-(4-pyridinyl)ethylamines
  2. Precursor for intermediates of highly stable chiral (A)6-B Supramolecular Copolymers

Chemical Properties

White needles

Uses

(1R)-1-(4-Pyridyl)ethanol is a building block reagent used in the synthesis of potent GPR119 receptor agonists used in the treatment of diabetes.

Purification Methods

Purify it by recrystallisation from pet ether. The m recorded after sublimation was 59.9-60.2o, and 55o after crystallisation from *C6H6/pet ether or pet ether/*C6H6. The (-)-di-O-benzoyl tartrate salt has m 146-148o (from EtOH). [UV, ORD: Harelli & Samori J Chem Soc Perkin Trans 2 1462 1974.] The racemate recrystallises from Et2O with m 74-76o,b 90-94o/1mm. The picrate has m 125-126o (from *C6H6). [Ferles & Attia Collect Czech Chem Commun 38 611 1973, UV, NMR: Nielson et al. J Org Chem 29 2898 1964, Beilstein 21 III/IV 522, 21/2 V 217.]

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