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Wholesale Price S-2-Amino-1-butanol - (R)-(+)-tert-Butylsulfinamide CAS 196929-78-9 Purity ≥99.0% e.e≥99.0% High Purity – Ruifu Featured Image
  • Wholesale Price S-2-Amino-1-butanol - (R)-(+)-tert-Butylsulfinamide CAS 196929-78-9 Purity ≥99.0% e.e≥99.0% High Purity – Ruifu

Wholesale Price S-2-Amino-1-butanol - (R)-(+)-tert-Butylsulfinamide CAS 196929-78-9 Purity ≥99.0% e.e≥99.0% High Purity – Ruifu

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Wholesale Price S-2-Amino-1-butanol - (R)-(+)-tert-Butylsulfinamide CAS 196929-78-9 Purity ≥99.0% e.e≥99.0% High Purity – Ruifu Detail:

Manufacturer Supply with High Purity and Stable Quality
(R)-(+)-tert-Butylsulfinamide CAS 196929-78-9
(S)-(-)-tert-Butylsulfinamide CAS 343338-28-3
Chiral Compounds, High Quality, Commercial Production

Chemical Name (R)-(+)-tert-Butylsulfinamide
Synonyms (R)-(+)-2-Methyl-2-Propanesulfinamide
CAS Number 196929-78-9
CAT Number RF-CC218
Stock Status In Stock, Production Scale Up to Tons
Molecular Formula C4H11NOS
Molecular Weight 121.2
Melting Point 103.0~107.0℃
Brand Ruifu Chemical
Item Specifications
Appearance White to Off-White Solid
Purity (LC-220nm) ≥99.0% 
E.E. (LC) ≥99.0% 
Specific Rotation +2.5° ~ +6.5° (C=1, CHCl3)
Test Standard Enterprise Standard
Usage Chiral Compounds; Pharmaceutical Intermediates 

Package: Bottle, Aluminium foil bag, Cardboard Drum, 25kg/Drum, or according to customer’s requirement.

Storage Condition: Store in sealed containers at cool and dry place; Protect from light, moisture and pest infestation.

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Shanghai Ruifu Chemical Co., Ltd. is the leading manufacturer and supplier of (R)-(+)-tert-Butylsulfinamide (CAS: 196929-78-9) with high quality, widely used in organic synthesis, synthesis of pharmaceutical intermediates and Active Pharmaceutical Ingredient (API) synthesis

Shanghai Ruifu Chemical Co., Ltd. plays an important role in the chiral chemistry, the company is committed to the production of chiral compounds. Our products are widely praised by customers.

(R)-(+)-2-Methyl-2-propanesulfinamide is a chiral ligand, which is used in pharmaceutical compositions. Further, it is used in the preparation of beta-chloro sulfinamides in the synthesis of chiral azridines. It is involved in the preparation of organocatalyst for enantioselective reduction of imines. It serves as a reagent for synthesizing chiral amines. In addition to this, it is converted into P,N-sulfinyl imine ligands through condensation with aldehydes and ketones which undergoes iridium-catalyzed asymmetric hydrogenation of olefins.

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