(S)-(-)-tert-Butylsulfinamide CAS 343338-28-3 Purity ≥99.0% e.e≥99.0% Manufacturer High Purity

Short Description:

Chemical Name: (S)-(-)-tert-Butylsulfinamide (S-BSN)

CAS: 343338-28-3

Appearance: White to Off-White Powder

Purity (LC): ≥99.0%

E.E. (LC): ≥99.0%

Chiral Compounds, High Quality, Commercial Production

E-Mail: alvin@ruifuchem.com

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Product Detail

Product Tags

Description:

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 Properties:

Chemical Name	(S)-(-)-tert-Butylsulfinamide
Synonyms	(S)-(-)-2-Methyl-2-Propanesulfinamide; S-BSN
CAS Number	343338-28-3
CAT Number	RF-CC219
Stock Status	In Stock, Production Scale Up to Tons
Molecular Formula	C4H11NOS
Molecular Weight	121.2
Melting Point	97.0~101.0℃
Solubility	Soluble in Methanol
Brand	Ruifu Chemical

Specifications:

Item	Specifications
Appearance	White to Off-White Powder
Specific Rotation	-2.5° ~ -6.5° (C=1, CHCl3)
Purity (LC)	≥99.0%
E.E (LC)	≥99.0%
Total Impurities	≤1.0%
Heavy Metals (as Pb)	≤20ppm
Test Standard	Enterprise Standard
Usage	Chiral Compounds; Pharmaceutical Intermediates

Package & Storage:

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.

Advantages:

FAQ:

Application:

Shanghai Ruifu Chemical Co., Ltd. is the leading manufacturer and supplier of (S)-(-)-tert-Butylsulfinamide (CAS: 343338-28-3) 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.

(S)-(-)-tert-Butylsulfinamide (CAS: 343338-28-3) 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.