missing translation for 'onlineSavingsMsg'
Learn More

(S)-(-)-2-Methyl-2-propanesulfinamide, 97%, Thermo Scientific Chemicals

Catalog Number 11436210
Click to view available options
Quantity:
1 g
5 g
25 g
This item is not returnable. View return policy
343338-28-3
C4H11NOS
121.198
MFCD05861480
CESUXLKAADQNTB-ZETCQYMHSA-N
s---2-methyl-2-propanesulfinamide, s-2-methylpropane-2-sulfinamide, s-tert-butanesulfinamide, s---tert-butanesulfinamide, s---t-butylsulfinamide, s---tert-butylsulfinamide, s-2-methyl-2-propanesulfinamide, s-tert-butylsulfinamide, s---t-butylmethylsulfinamide, s-t-butyl sulfinamide
11355477
2-methylpropane-2-sulfinamide
CC(C)(C)S(=O)N
This item is not returnable. View return policy
343338-28-3
C4H11NOS
121.198
MFCD05861480
CESUXLKAADQNTB-ZETCQYMHSA-N
s---2-methyl-2-propanesulfinamide, s-2-methylpropane-2-sulfinamide, s-tert-butanesulfinamide, s---tert-butanesulfinamide, s---t-butylsulfinamide, s---tert-butylsulfinamide, s-2-methyl-2-propanesulfinamide, s-tert-butylsulfinamide, s---t-butylmethylsulfinamide, s-t-butyl sulfinamide
11355477
2-methylpropane-2-sulfinamide
CC(C)(C)S(=O)N

(S)-(-)-2-Methyl-2-propanesulfinamide is used in Suzuki reaction. It is also employed as a reagent for synthesizing chiral amines. It acts as a chiral auxiliary used in an asymmetric synthesis of trifluoroethylamines by conversion of trifluoroacetaldehyde to a chiral imine. It is also involved in the transformation of P,N-sulfinyl imine ligands through condensation with aldehydes and ketones, which can undergo iridium-catalyzed asymmetric hydrogenation of olefins. Further, it serves as a reagent for the preparation of chemicals and pharmaceutical intermediates.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
(S)-(-)-2-Methyl-2-propanesulfinamide is used in Suzuki reaction. It is also employed as a reagent for synthesizing chiral amines. It acts as a chiral auxiliary used in an asymmetric synthesis of trifluoroethylamines by conversion of trifluoroacetaldehyde to a chiral imine. It is also involved in the transformation of P,N-sulfinyl imine ligands through condensation with aldehydes and ketones, which can undergo iridium-catalyzed asymmetric hydrogenation of olefins. Further, it serves as a reagent for the preparation of chemicals and pharmaceutical intermediates.

Notes
Incompatible with strong oxidizing agents. Store in a cool place.
TRUSTED_SUSTAINABILITY
Melting Point 97°C to 101°C
Quantity 5 g
Formula Weight 121.2
Percent Purity 97%
Chemical Name or Material (S)-(-)-2-Methyl-2-propanesulfinamide

RUO – Research Use Only

missing translation for 'provideContentCorrection'

missing translation for 'productTitle'