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

2-Cloropiridina, 99 %, Thermo Scientific Chemicals

CAS: 109-09-1 | C5H4ClN | 113.544 g/mol
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Cantidad:
100 g
500 g
Número de catálogo A14866.36
también denominado A14866-36
Precio (USD)
-
Cantidad:
500 g
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Identificadores químicos
CAS109-09-1
IUPAC Name2-chloropyridine
Molecular FormulaC5H4ClN
InChI KeyOKDGRDCXVWSXDC-UHFFFAOYSA-N
SMILESClC1=CC=CC=N1
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EspecificacionesSpecification SheetHoja de especificaciones
FormLiquid
Refractive Index1.5315-1.5345 @ 20?C
Appearance (Color)Clear colorless to pale yellow
Assay (GC)≥98.5%
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.

Aplicaciones
La 2-cloropiridina se utiliza como producto químico intermedio en la producción de varias piritionas, para su uso en cosméticos, productos de cuidado personal y productos farmacéuticos.

Solubilidad
Soluble en agua (27 g/l).

Notas
Mantenga el recipiente bien cerrado. Almacénese lejos de los agentes oxidantes.
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.