CAS 17880-61-4

methyl 5-ethynylpicolinate

Description:

Methyl 5-ethynylpicolinate, with the CAS number 17880-61-4, is an organic compound that belongs to the class of picolinates, which are derivatives of pyridine. This compound features a methyl ester functional group and an ethynyl group, contributing to its unique reactivity and properties. It typically appears as a colorless to pale yellow liquid or solid, depending on its purity and form. Methyl 5-ethynylpicolinate is known for its potential applications in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals, due to the presence of the ethynyl group, which can participate in various coupling reactions. The compound is also characterized by its relatively low solubility in water but good solubility in organic solvents, making it useful in various chemical processes. Safety data should be consulted for handling and storage, as with many organic compounds, it may pose health risks if not managed properly. Overall, methyl 5-ethynylpicolinate is a versatile compound with significant implications in synthetic organic chemistry.

2-Pyridinecarboxylic acid, 5-ethynyl-, methyl ester

CAS: 17880-61-4

Formula: C₉H₇NO₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 161.1574

Ref: IN-DA0026BU

Methyl 5-ethynylpyridine-2-carboxylate

CAS: 17880-61-4

Purity: >95%

Molecular weight: 161.157

Ref: FT-M13967

Methyl 5-ethynylpyridine-2-carboxylate

CAS: 17880-61-4

Methyl 5-ethynylpyridine-2-carboxylate

Formula: C₉H₇NO₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 161.16g/mol

Ref: 54-OR52206

Methyl 5-ethynylpyridine-2-carboxylate

CAS: 17880-61-4

Formula: C₉H₇NO₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 161.16

Ref: 10-F330703

Methyl 5-ethynylpyridine-2-carboxylate

CAS: 17880-61-4

Methyl 5-ethynylpyridine-2-carboxylate is a ligand that binds in the active site of many enzymes. It can enhance the activity of these enzymes and also change their conformations. Methyl 5-ethynylpyridine-2-carboxylate interacts with four subunits to form a tetradentate framework, which is responsible for this molecule's ability to bind to any type of ligand. This enhancement effect is reversible, and it can be reversed by oxidizing methyl 5-ethynylpyridine-2-carboxylate with nitric acid. The yield of methyl 5-ethynylpyridine-2-carboxylate depends on the reaction conditions and the type of arylacetylene used. Methyl 5-ethynylpyridine-2-carboxylate has been shown to be an effective ligand with a high emission yield when using 1,3

Formula: C₉H₇NO₂

Purity: Min. 95%

Molecular weight: 161.2 g/mol

Ref: 3D-SAA88061