154369
2,6-Pyridinedimethanol
98%
Synonym(s):
2,6-Bis(hydroxymethyl)pyridine
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About This Item
Recommended Products
Quality Level
Assay
98%
form
powder
mp
112-114 °C (lit.)
SMILES string
OCc1cccc(CO)n1
InChI
1S/C7H9NO2/c9-4-6-2-1-3-7(5-10)8-6/h1-3,9-10H,4-5H2
InChI key
WWFMINHWJYHXHF-UHFFFAOYSA-N
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Application
2,6-Pyridinedimethanol can be used as a ligand to synthesize a variety of metal complexes and catalysts. It can also be used as a reactant to prepare Fe(III) complexes [Fe(18)O(6)(OH)(8)(pdm)(10)(pdmH)(4)(H(2)O)(4)](ClO(4))(10) and [Fe(9)O(4)(OH)(2)(O(2)CMe)(10)(pdm)(pdmH)(4)](NO(3)).
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Catalysis Today, 121, 140-140 (2007)
Dalton transactions (Cambridge, England : 2003), 39(38), 9131-9139 (2010-09-08)
The syntheses, crystal structures and magnetochemical characterization are reported for two new Fe(III) complexes [Fe(18)O(6)(OH)(8)(pdm)(10)(pdmH)(4)(H(2)O)(4)](ClO(4))(10) (3) and [Fe(9)O(4)(OH)(2)(O(2)CMe)(10)(pdm)(pdmH)(4)](NO(3)) (4). They were synthesized from the use of the potentially O,N,O tridentate chelate, 2,6-pyridinedimethanol (pdmH(2)), in the presence or absence of carboxylate
Large bite bisphosphite, 2,6-C5H3N{CH2OP(?OC10H6)(?-S)(C10H6O?)}2: Synthesis, derivatization, transition metal chemistry and application towards hydrogenation of olefins
Journal of Organometallic Chemistry, 692, 1683-1689 (2007)
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