586-98-1
Chemical Structure
2-Pyridinemethanol
- CAS No.: 586-98-1
- Formula:C6H7NO
- Molecular Weight:109.13
IUPAC Name: pyridin-2-ylmethanol
InChIKey: SHNUBALDGXWUJI-UHFFFAOYSA-N
SMILES: OCC1=NC=CC=C1
Biological Activity: 2-Pyridinemethanol acts as a chelating auxiliary, co-catalyst and ligand, with pH-dependent coordination capacity for Cu (II) ions. 2-Pyridinemethanol can be used in combination with Acetylcholine (HY-B0282) and Pyridostigmine (HY-B0207A) for research related to obstructive arthropathy[1][2][3].
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2-Pyridinemethanol | 99.98% | 2-Pyridinemethanol acts as a chelating auxiliary, co-catalyst and ligand, with pH-dependent coordination capacity for Cu (II) ions. 2-Pyridinemethanol can be used in combination with Acetylcholine (HY-B0282) and Pyridostigmine (HY-B0207A) for research related to obstructive arthropathy. | ||||||||||||||||||||
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2-Pyridinemethanol (Standard) | ≥98% | 2-Pyridinemethanol (Standard) is the analytical standard of 2-Pyridinemethanol (HY-Y0004). This product is intended for research and analytical applications. 2-Pyridinemethanol acts as a chelating auxiliary, co-catalyst and ligand, with pH-dependent coordination capacity for Cu (II) ions. 2-Pyridinemethanol can be used in combination with Acetylcholine (HY-B0282) and Pyridostigmine (HY-B0207A) for research related to obstructive arthropathy. | ||||||||||||||||||||
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[1]. BARONI GC, CIPRIANI D. [Obliterative arthropathies. Clinical findings and current status; the combination of acetylcholine, 2-pyridinemethanol and pyridostigmine in their therapy]. Clin Ter. 1959 Aug;17:135-72. Italian.
- [2]. Kim DS, et al. Hydroesterification of alkenes with sodium formate and alcohols promoted by cooperative catalysis of Ru3(CO)12 and 2-pyridinemethanol. The Journal of organic chemistry. 2014 Dec 19;79(24):12191-6. [Content Brief]
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[3]. Hamaguchi T, et al. pH-Dependent structural diversity of a 2-pyridinemethanol Cu complex and its relatively strong magnetic exchange coupling via hydrogen bonding. Dalton Trans. 2017 May 16;46(19):6196-6201.