Promotional price valid on web orders only. Your contract pricing may differ. Interested in signing up for a dedicated account number?
Learn More

(S)-(-)-2-Methyl-2-propanesulfinamide, 97%

Catalog No. AAH2711503
Change view
Click to view available options
Quantity:
1 g
5 g
25 g
3 product options available for selection
Product selection table with 3 available options. Use arrow keys to navigate and Enter or Space to select.
Catalog No. Quantity
AAH2711503 1 g
AAH2711506 5 g
AAH2711514 25 g
Use arrow keys to navigate between rows. Press Enter or Space to select a product option. 3 options available.
3 options
Catalog No. AAH2711503 Supplier Thermo Scientific Chemicals Supplier No. H2711503
Only null left
Add to Cart

CAS: 343338-28-3 | C4H11NOS | 121.198 g/mol

(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

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

Specifications

Melting Point 97°C to 101°C
Quantity 1 g
Formula Weight 121.2
Percent Purity 97%
Chemical Name or Material (S)-(-)-2-Methyl-2-propanesulfinamide
TSCA No
Recommended Storage Keep cold

RUO – Research Use Only

Product Title
Select an issue

By clicking Submit, you acknowledge that you may be contacted by Fisher Scientific in regards to the feedback you have provided in this form. We will not share your information for any other purposes. All contact information provided shall also be maintained in accordance with our Privacy Policy.