Search

  • Order Status
  • Quick Order
  • Promos
Element SearchElement SearchStructure SearchStructure Search
4-Chloropyridine hydrochloride, 98+%
4-Chloropyridine hydrochloride, 98+%
4-Chloropyridine hydrochloride, 98+%
Thermo Scientific Chemicals

4-Chloropyridine hydrochloride, 98+%

CAS: 7379-35-3 | C5H5Cl2N | 150.00 g/mol
Have Questions?
Change viewbuttonViewtableView
Quantity:
5 g
25 g
100 g
ChemDexTry the chem dexTM web app
Catalog number A15628.06
also known as A15628-06
Price (EUR)
25,30
Each
Quantity:
5 g
Request bulk or custom format
Price (EUR)
25,30
Each
Chemical Identifiers
CAS7379-35-3
IUPAC Namehydrogen 4-chloropyridine chloride
Molecular FormulaC5H5Cl2N
InChI KeyXGAFCCUNHIMIRV-UHFFFAOYSA-N
SMILES[H+].[Cl-].ClC1=CC=NC=C1
View more
SpecificationsSpecification SheetSpecification Sheet
FormCrystals or powder or crystalline powder
Identification (FTIR)Conforms
Appearance (Color)White to cream or pale yellow
Assay (Titration ex Chloride)≥98.0 to ≤102.0%
It is employed as a catalyst in the synthesis of fluorazone derivatives by one-pot pyrrolation/cyclization of anthranilic acids.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
It is employed as a catalyst in the synthesis of fluorazone derivatives by one-pot pyrrolation/cyclization of anthranilic acids.

Solubility
Soluble in water.

Notes
Store away from oxidizing agents. Keep the container tightly closed and place it in a cool, dry and well ventilated condition.
RUO – Research Use Only

General References:

  1. Francesca Aiello, et al. Convenient synthesis of fluorazone derivatives by one-pot pyrrolation/cyclization of anthranilic acids.Tetrahedron Lett.,2011,52(44), 5824-5826.
  2. Ghislaine Priem, et al. A simple and effective synthetic approach to chiral 4-pyridinyl proline derivatives.Tetrahedron Lett.,2002,43(34), 6001-6003.
  3. For a study of regioselective metallation reactions, see: Heterocycles, 35, 151 (1993).