[H27115] CAS 343338-28-3 | (S)-(-)-2-Methyl-2-propanesulfinamide, 97% | Alfa
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Brand: Alfa Aesar
343338-28-3 | C4H11NOS | tert-butanesulfinamide
Chemical Identifiers
CAS
343338-28-3
Molecular Weight (g/mol)
121.20
Synonym
tert-butanesulfinamide
SMILES
CC(C)(C)S(N)=O
InChI Key
CESUXLKAADQNTB-UHFFFAOYNA-N
Molecular Formula
C4H11NOS
IUPAC Name
2-methylpropane-2-sulfinamide
Specifications
Appearance (Color)
White to pale cream or to pale yellow
Form
crystalline solid/powder
Assay (GC)
> 96.0%
Enantiomeric excess
>99.0%
설명
(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.
(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.
GHS Hazard and Precautionary Statements
Hazard Statements:
Risk & Safety
TSCA:No
경고:RUO – Research Use Only
CAS343338-28-3FORMULAC4H11NOSMDLMFCD05861480
| Pakage | 1g, 25g, 5g |
|---|---|
| brand | Alfa Aesar |
