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

78.89 € - 839.18 €

Chemical Identifiers

CAS 343338-28-3
Molecular Formula C4H11NOS
Molecular Weight (g/mol) 121.198
MDL Number MFCD05861480
InChI Key CESUXLKAADQNTB-ZETCQYMHSA-N
Synonym 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
PubChem CID 11355477
IUPAC Name 2-methylpropane-2-sulfinamide
SMILES CC(C)(C)S(=O)N
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Thermo Scientific Alfa Aesar
H27115.03
1 g
78.89 €
1g
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11436210
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Thermo Scientific Alfa Aesar
H27115.06
5 g
219.09 €
5g
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11446210
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Thermo Scientific Alfa Aesar
H27115.14
25 g
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Description

Description

(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.
Specifications
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Safety and Handling

Safety and Handling

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Recommended Storage : Keep cold

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RUO – Research Use Only

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