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2-Methoxypyridin-3-amine

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2-Methoxypyridin-3-amine Basic information

Product Name:
2-Methoxypyridin-3-amine
Synonyms:
  • 2-METHOXYPYRIDIN-3-AMINE
  • 2-METHOXY-PYRIDIN-3-YLAMINE
  • TIMTEC-BB SBB005483
  • BUTTPARK 37\08-36
  • 3-AMINO-2-METHOXYPYRIDINE
  • 2-Methoxy-3-aminopyridine
  • 2-Methoxypyridine-3-amine
  • 3-AMINO-2-METHOXYPYRIDINE 98+%
CAS:
20265-38-7
MF:
C6H8N2O
MW:
124.14
EINECS:
673-107-9
Product Categories:
  • Pyridines
  • Amines
  • pharmacetical
  • Pyridine series
  • Pyridine
Mol File:
20265-38-7.mol
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2-Methoxypyridin-3-amine Chemical Properties

Melting point:
67 °C
Boiling point:
118°C/13mmHg(lit.)
Density 
1.139±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
solubility 
soluble in Methanol
form 
powder to crystal
pka
4.33±0.10(Predicted)
color 
Orange to Brown to Dark red
InChI
InChI=1S/C6H8N2O/c1-9-6-5(7)3-2-4-8-6/h2-4H,7H2,1H3
InChIKey
YXFAOWYMDGUFIQ-UHFFFAOYSA-N
SMILES
C1(OC)=NC=CC=C1N
CAS DataBase Reference
20265-38-7(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
20/21/22-36/37/38-41-37/38-22
Safety Statements 
26-36/37/39-39
HazardClass 
IRRITANT
HS Code 
29339900
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2-Methoxypyridin-3-amine Usage And Synthesis

Uses

2-Methoxy-3-aminopyridine can be used as an intermediate in pharmaceutical chemistry and organic synthesis. In synthetic transformations, the amino group on the pyridine ring can be diazotized and then further derivatized, for example, by in-situ reduction to hydrazine compounds. Furthermore, under appropriate halogenation conditions, a halogen atom can be introduced at the fourth position of pyridine.

Chemical Properties

Reddish brown solid

Definition

ChEBI: 2-Methoxypyridin-3-amine is an aminopyridine.

References

[1] Tetrahedron, 1997, vol. 53, # 37, p. 12505 - 12524
[2] Patent: US2011/237791, 2011, A1. Location in patent: Page/Page column 63
[3] Patent: US5652363, 1997, A
[4] Patent: WO2005/26137, 2005, A2. Location in patent: Page/Page column 233
[5] Bulletin de la Societe Chimique de France, 1992, # 1, p. 79 - 84

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