(R)-Tetrahydro-3H-pyrrolo[1,2-c][1,2,3]oxathiazole 1,1-dioxide

≥95%

Reagent Code: #230516
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CAS Number 143577-46-2

science Other reagents with same CAS 143577-46-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 163.20 g/mol
Formula C₅H₉NO₃S
badge Registry Numbers
MDL Number MFCD26406787
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used as a chiral auxiliary or intermediate in asymmetric synthesis, particularly in the development of biologically active compounds. Its rigid, fused ring structure with defined stereochemistry makes it valuable for controlling stereoselectivity in reactions such as alkylations, aldol additions, and cyclizations. Commonly employed in pharmaceutical research to construct enantiomerically pure nitrogen- and sulfur-containing heterocycles. The sulfonamide group allows for further functionalization or coordination, enhancing its utility in catalyst design and medicinal chemistry.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿5,220.00
250mg
10-20 days ฿10,440.00
(R)-Tetrahydro-3H-pyrrolo[1,2-c][1,2,3]oxathiazole 1,1-dioxide
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Used as a chiral auxiliary or intermediate in asymmetric synthesis, particularly in the development of biologically active compounds. Its rigid, fused ring structure with defined stereochemistry makes it valuable for controlling stereoselectivity in reactions such as alkylations, aldol additions, and cyclizations. Commonly employed in pharmaceutical research to construct enantiomerically pure nitrogen- and sulfur-containing heterocycles. The sulfonamide group allows for further functionalization or coord

Used as a chiral auxiliary or intermediate in asymmetric synthesis, particularly in the development of biologically active compounds. Its rigid, fused ring structure with defined stereochemistry makes it valuable for controlling stereoselectivity in reactions such as alkylations, aldol additions, and cyclizations. Commonly employed in pharmaceutical research to construct enantiomerically pure nitrogen- and sulfur-containing heterocycles. The sulfonamide group allows for further functionalization or coordination, enhancing its utility in catalyst design and medicinal chemistry.

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