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900761

Sigma-Aldrich

Sodium 4-methylpyridine-2-sulfinate

≥95%

Synonym(s):

Willis 4-methyl pyridine-2-sulfinate

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About This Item

Empirical Formula (Hill Notation):
C6H6NNaO2S
Molecular Weight:
179.17
UNSPSC Code:
12352200

Assay

≥95%

form

powder or crystals

reaction suitability

reaction type: C-C Bond Formation

mp

342 °C

Application

This 2-pyridylsulfinate enables Suzuki-Miyaura cross coupling with aryl halides to access diverse pyridine derivatives as reported by the laboratory of Michael Willis.. No longer impeded by unstable 2-pyridyl boronates, the sulfinate alternatives provide Pd-catalyzed coupling routes to therapeutically valuable pyridine rings.

Other Notes

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

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Articles

Willis Pyridinates for Palladium-Catalyzed Cross-Coupling Reactions

Description: Professor Willis and partners at Pfizer have shown with pyridine-2- sulfinates a palladium-catalyzed desulfinylative cross-coupling process can be realized.

Willis Pyridinates for Palladium-Catalyzed Cross-Coupling Reactions

Description: Professor Willis and partners at Pfizer have shown with pyridine-2- sulfinates a palladium-catalyzed desulfinylative cross-coupling process can be realized.

Willis Pyridinates for Palladium-Catalyzed Cross-Coupling Reactions

Description: Professor Willis and partners at Pfizer have shown with pyridine-2- sulfinates a palladium-catalyzed desulfinylative cross-coupling process can be realized.

Willis Pyridinates for Palladium-Catalyzed Cross-Coupling Reactions

Description: Professor Willis and partners at Pfizer have shown with pyridine-2- sulfinates a palladium-catalyzed desulfinylative cross-coupling process can be realized.

Related Content

Willis Group – Professor Product Portal

Research in the Willis group is focused on the development of new catalysts and reactions for synthetic chemistry. The group is particularly interested in addressing synthetic challenges that are applicable to the pharmaceutical and agrochemical industries.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

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