2-Chloropyridine, 99%
2-Chloropyridine, 99%
2-Chloropyridine, 99%
2-Chloropyridine, 99%
Thermo Scientific Chemicals

2-Chloropyridine, 99%

CAS: 109-09-1 | C5H4ClN | 113.544 g/mol
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Catalog NumberQuantity
ALFA14866.22100 g
Catalog number ALFA14866.22
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Quantity:
100 g
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Specifications
Chemical Name or Material2-Chloropyridine
CAS109-09-1
Health Hazard 1H227-H302-H310+H330-H315-H318-H373
Health Hazard 2GHS H Statement
H301-H310-H330-H318-H227-H315-H335
Toxic if swallowed.
Fatal in contact with skin.
Fatal if inhaled.
Causes serious eye damage.
Combustible liquid.
Causes skin irritation.
May cause respiratory irritation.
Health Hazard 3P210-P235-P260-P262-P264b-P270-P271-P280-P284-P301+P312-P302+P350-P304+P340-P305+P351+P338-P310-P314-P330-P332+P313-P361-P363-P370+P378q-P501c
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2- Chloropyridine is used as an intermediate chemical in the production of various pyrithione, for use in cosmetics, personal care products and pharmaceutical products.

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
2- Chloropyridine is used as an intermediate chemical in the production of various pyrithione, for use in cosmetics, personal care products and pharmaceutical products.

Solubility
Soluble in water (27g/L).

Notes
Keep container tightly closed. Store away from oxidizing agents.
RUO – Research Use Only

General References:

  1. Sabine Choppin.; Philippe Gros.; Yves For. Unusual C-6 Lithiation of 2-Chloropyridine-Mediated by BuLi-Me2N(CH2)2OLi. New Access to 6-Functional-2-chloropyridines and Chloro-bis-heterocycles. Org. Lett. 2002, 2, (6), 803-805.
  2. Meriç Bakiler.; I.V. Maslov.; Sevim Akyüzc.Theoretical study of the vibrational spectra of 2-chloropyridine metal complexes. I. Calculation and analysis of the IR spectrum of 2-chloropyridine. Journal of Molecular Structure. 1999, 475, (1), 83-92.
  3. Reaction with the unimetal suberbase complex formed from 2 mol of n-BuLi and I mol of 2-(Dimethyl amino) ethanol, B23616, in hexane, gives products resulting from apparent metallation at the 6-position, providing useful access to 6-functionalized 2-chloropyridines: Org. Lett., 2, 803 (2000). See also 2-Methoxypyridine, A13675, for a similar effect.