CAS 42330-59-6
:2-Chloro-3-pyridinemethanol
- (2-Chloropyridin-3-Yl)Methanol
- 2-Chloro-3-(hydroxymethyl)pyridine
- 2-Chloro-3-hydroxymethylpyridine
- 2-Chloro-3-pyridinemethanol
- 2-Chloro-3-pyridylmethanol
- 2-Choro-3-(hydroxymethyl)pyridine
- 3-Pyridinemethanol, 2-chloro-
- (2-Chloro-3-pyridinyl)methanol
- 2-Chloro-3-Pyridinyl Methanol
2-Chloro-3-pyridinemethanol, 97%
CAS: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 Sci
Formula:C6H6ClNOPurity:97%Molecular weight:143.572-Chloro-3-pyridinylmethanol
CAS:Formula:C6H6ClNOPurity:97%Color and Shape:SolidMolecular weight:143.57092-Chloro-3-(hydroxymethyl)pyridine
CAS:2-Chloro-3-(hydroxymethyl)pyridineFormula:C6H6ClNOPurity:98%Color and Shape: beige solidMolecular weight:143.57g/mol(2-Chloropyridin-3-yl)methanol
CAS:Formula:C6H6ClNOPurity:98%Color and Shape:SolidMolecular weight:143.572-Chloro-3-(hydroxymethyl)pyridine
CAS:2-Chloro-3-(hydroxymethyl)pyridine is an organic compound that is used as a building block for the synthesis of other heterocycles. This compound can be synthesized from 2-chloronicotinic acid, which is obtained by oxidation of nicotine with sodium hypochlorite in the presence of potassium ion. The reaction proceeds via a cleavage of the C-Cl bond and formation of a pyridine ring. The catalytic process can be performed at room temperature and at atmospheric pressure in a variety of solvents, including water.
2-Chloro-3-(hydroxymethyl)pyridine has been shown to have high yields for the preparation of compounds such as 2,4-dichloropyridine and 4,5-dichloropyrimidine. It also has been used in the preparation of pharmaceuticals such as atrial natriuretic factor (ANF).Formula:C6H6ClNOPurity:Min. 98 Area-%Color and Shape:PowderMolecular weight:143.57 g/mol




