(R)-N-(cyclopropylmethylene)-2-methylpropane-2-sulfinamide

≥95%

Reagent Code: #229575
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CAS Number 1087348-60-4

science Other reagents with same CAS 1087348-60-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 173.28 g/mol
Formula C₈H₁₅NOS
inventory_2 Storage & Handling
Storage 2-8 °C, sealed, dry

description Product Description

Used as a chiral auxiliary in asymmetric synthesis, enabling the selective formation of enantiomerically enriched amines and amino acid derivatives. Its structure facilitates high stereocontrol in nucleophilic addition reactions, particularly in the synthesis of biologically active molecules such as pharmaceuticals and agrochemicals. Commonly employed in the preparation of chiral intermediates via Ellman’s sulfinimine chemistry, allowing efficient access to primary and secondary amines with excellent enantiomeric purity. Widely applied in medicinal chemistry for the development of optically active drugs, including protease inhibitors and central nervous system agents.

Available Sizes & Pricing

Size Availability Unit Price Quantity
200mg
10-20 days ฿7,060.00
(R)-N-(cyclopropylmethylene)-2-methylpropane-2-sulfinamide
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Used as a chiral auxiliary in asymmetric synthesis, enabling the selective formation of enantiomerically enriched amines and amino acid derivatives. Its structure facilitates high stereocontrol in nucleophilic addition reactions, particularly in the synthesis of biologically active molecules such as pharmaceuticals and agrochemicals. Commonly employed in the preparation of chiral intermediates via Ellman’s sulfinimine chemistry, allowing efficient access to primary and secondary amines with excellent enanti
Used as a chiral auxiliary in asymmetric synthesis, enabling the selective formation of enantiomerically enriched amines and amino acid derivatives. Its structure facilitates high stereocontrol in nucleophilic addition reactions, particularly in the synthesis of biologically active molecules such as pharmaceuticals and agrochemicals. Commonly employed in the preparation of chiral intermediates via Ellman’s sulfinimine chemistry, allowing efficient access to primary and secondary amines with excellent enantiomeric purity. Widely applied in medicinal chemistry for the development of optically active drugs, including protease inhibitors and central nervous system agents.
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