Basic information Safety Supplier Related

4-AMIDINOPYRIDINE HYDROCHLORIDEPYRIDINE-4-CARBOXIMIDAMIDE HYDROCHLORIDE

Basic information Safety Supplier Related

4-AMIDINOPYRIDINE HYDROCHLORIDEPYRIDINE-4-CARBOXIMIDAMIDE HYDROCHLORIDE Basic information

Product Name:
4-AMIDINOPYRIDINE HYDROCHLORIDEPYRIDINE-4-CARBOXIMIDAMIDE HYDROCHLORIDE
Synonyms:
  • 4-AMIDINOPYRIDINE HYDROCHLORIDE, 98+%
  • 4-pyridin-carbamidine hydrochloride
  • IsonicotiniMidaMide hydrochloride
  • Pyridine-4-carboximidamide hydrochloride, 4-Carbamimidoylpyridine hydrochloride, Pyridine-4-carboxamidine hydrochloride
  • 4-AMIDINOPYRIDINE HYDROCHLORIDEPYRIDINE-4-CARBOXIMIDAMIDE HYDROCHLORIDE
  • 4-Amidinopyridinium chloride, 98+%
  • 4-AmidinopyridiniumHCl
  • 4-pyridinecarboxamidine hydrochloride
CAS:
6345-27-3
MF:
C12H16Cl2N6
MW:
315.20164
Mol File:
6345-27-3.mol
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4-AMIDINOPYRIDINE HYDROCHLORIDEPYRIDINE-4-CARBOXIMIDAMIDE HYDROCHLORIDE Chemical Properties

Melting point:
240-242°C
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
Appearance
White to off-white Solid
Sensitive 
Hygroscopic
BRN 
3562678
InChI
InChI=1S/2C6H7N3.2ClH/c2*7-6(8)5-1-3-9-4-2-5;;/h2*1-4H,(H3,7,8);2*1H
InChIKey
YXRVCYDHRUUPFU-UHFFFAOYSA-N
SMILES
C1N=CC=C(C(=N)N)C=1.[H]Cl.C1N=CC=C(C(N)=N)C=1.[H]Cl
CAS DataBase Reference
6345-27-3
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36-37
Hazard Note 
Irritant
HS Code 
29333990
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4-AMIDINOPYRIDINE HYDROCHLORIDEPYRIDINE-4-CARBOXIMIDAMIDE HYDROCHLORIDE Usage And Synthesis

Chemical Properties

White powder

Synthesis

100-48-1

6345-27-3

The general procedure for the synthesis of 4-formamidopyridine hydrochloride from 4-cyanopyridine was as follows: 4-cyanopyridine (20.0 g, 0.2 mol) was dissolved in anhydrous methanol (200 mL), followed by a one-time addition of powdered sodium methanol (1.1 g, 20 mmol). The reaction mixture was stirred at room temperature overnight. Next, ammonium chloride (16.5 g, 0.31 mol) was added and the reaction mixture was heated to reflux for 4 hours, after which it was cooled to room temperature. The solvent was removed by evaporation, anhydrous ethanol (300 mL) was added, and the mixture was subsequently heated to reflux. after 15 min, the solid insoluble material was removed by filtration, and the filtrate was cooled to room temperature and allowed to stand overnight. The filtrate was filtered again to remove additional inorganic salts and finally the reaction mixture was concentrated to about one-third of the original volume, which was filtered to give 24.0 g of 4-formamidinopyridine hydrochloride in 76% yield.

References

[1] Bioorganic and Medicinal Chemistry Letters, 2016, vol. 26, # 15, p. 3487 - 3490
[2] Bioorganic and Medicinal Chemistry, 2011, vol. 19, # 11, p. 3347 - 3356
[3] Bioorganic and Medicinal Chemistry Letters, 2005, vol. 15, # 12, p. 2990 - 2993
[4] Journal of Medicinal Chemistry, 1990, vol. 33, # 4, p. 1230 - 1241
[5] Patent: US5294612, 1994, A

4-AMIDINOPYRIDINE HYDROCHLORIDEPYRIDINE-4-CARBOXIMIDAMIDE HYDROCHLORIDESupplier

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