New Arrival China L-(-)-Malic Acid Diethyl Ester - (R)-(+)-tert-Butylsulfinamide CAS 196929-78-9 Purity ≥99.0% e.e≥99.0% Manufacturer High Purity – Ruifu

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New Arrival China L-(-)-Malic Acid Diethyl Ester - (R)-(+)-tert-Butylsulfinamide CAS 196929-78-9 Purity ≥99.0% e.e≥99.0% Manufacturer 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; R-BSN
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℃
Solubility	Soluble in Methanol
Brand	Ruifu Chemical

Item	Specifications
Appearance	White to Off-White Powder
Purity (LC-220nm)	≥99.0%
E.E. (LC)	≥99.0%
Specific Rotation	+2.5° ~ +6.5° (C=1, CHCl3)
Single Impurity	≤0.50%
Total Impurities	<1.00%
Heavy Metals (as Pb)	<20ppm
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.

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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