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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 |
Product Code | Brand | Quantity | Price | Quantity & Availability | |||||
---|---|---|---|---|---|---|---|---|---|
Product Code | Brand | Quantity | Price | Quantity & Availability | |||||
11426210
|
Thermo Scientific Alfa Aesar
H27115.03 |
1 g |
78.89 €
1g |
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11436210
|
Thermo Scientific Alfa Aesar
H27115.06 |
5 g |
219.09 €
5g |
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11446210
|
Thermo Scientific Alfa Aesar
H27115.14 |
25 g |
839.18 €
25g |
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Descripción
(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.
Identificadores de productos químicos
343338-28-3 | |
121.198 | |
CESUXLKAADQNTB-ZETCQYMHSA-N | |
11355477 | |
CC(C)(C)S(=O)N |
C4H11NOS | |
MFCD05861480 | |
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 | |
2-methylpropane-2-sulfinamide |
Especificaciones
343338-28-3 | |
C4H11NOS | |
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 | |
CC(C)(C)S(=O)N | |
121.198 | |
121.2 | |
(S)-(-)-2-Methyl-2-propanesulfinamide |
97°C to 101°C | |
MFCD05861480 | |
CESUXLKAADQNTB-ZETCQYMHSA-N | |
2-methylpropane-2-sulfinamide | |
11355477 | |
97% |
Seguridad y manipulación
missing translation for 'tsca' : No
Recommended Storage : Keep cold
RUO – Research Use Only
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