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560871 Aldrich

2-Methyl-2-propanesulfinamide

97%, racemic

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Properties

Related Categories Building Blocks, Chemical Synthesis, Organic Building Blocks, Sulfonamides/Sulfinamides, Sulfur Compounds More...
InChI Key   CESUXLKAADQNTB-UHFFFAOYSA-N
assay   97%
mp   97-101 °C(lit.)
storage temp.   2-8°C

Description

Application

Synthesis of 4-sulfonyliminopiperidine and its reaction with benzyl Grignard to form an important pharmaceutical building block, 4-benzyl-4-aminopiperidne. Also used to prepare spiro tosylaziridines via methylene insertion into the derived sulfonylimine.

Ellman′s Sulfinamides

Packaging

1, 5, 25 g in poly bottle

Price and Availability

Safety & Documentation

Safety Information

RIDADR 
NONH for all modes of transport
WGK Germany 
3

Documents

Certificate of Analysis

Protocols & Articles

Articles

Ellman Group – Professor and Product Portal

From our library of Articles, Sigma-Aldrich presents Ellman Group – Professor and Product Portal
Keywords: Arylations, Asymmetric synthesis, C-C bond formation, Catalysis, Drug discovery, Ligands, Pharmaceutical

Related Content

Ellman's Sulfinamides in chemical Synthesis

Since its introduction by Ellman in 1997 as a chiral ammonia equivalent,1 enantiopure 2-methyl-2-propanesulfinamide (tert-butanesulfinamide) has been demonstrated to be a versatile chiral auxiliary a...
Keywords: Antibiotics, Asymmetric synthesis, Condensations, Cyclizations, Ligands, Reductions

Peer-Reviewed Papers
15

References

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