tert-Butyl (R)-4-((benzyloxy)methyl)-1,2,3-oxathiazolidine-3-carboxylate 2,2-dioxide

95%

Reagent Code: #153198
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CAS Number 2476729-51-6

science Other reagents with same CAS 2476729-51-6

blur_circular Chemical Specifications

inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as a chiral building block in the synthesis of biologically active molecules, particularly in the development of pharmaceuticals. Its protected amine and hydroxyl functionalities make it valuable in peptide-like structures and beta-amino alcohol synthesis. Commonly employed in asymmetric synthesis due to the stable chiral center, enabling selective formation of desired stereoisomers. The sulfonyl group enhances reactivity and directs selective transformations, useful in medicinal chemistry for constructing protease inhibitors or enzyme modulators.

Available Sizes & Pricing

Size Availability Unit Price Quantity
50mg
10-20 days ฿10,060.00
100mg
10-20 days ฿18,020.00
250mg
10-20 days ฿35,780.00
tert-Butyl (R)-4-((benzyloxy)methyl)-1,2,3-oxathiazolidine-3-carboxylate 2,2-dioxide
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Used as a chiral building block in the synthesis of biologically active molecules, particularly in the development of pharmaceuticals. Its protected amine and hydroxyl functionalities make it valuable in peptide-like structures and beta-amino alcohol synthesis. Commonly employed in asymmetric synthesis due to the stable chiral center, enabling selective formation of desired stereoisomers. The sulfonyl group enhances reactivity and directs selective transformations, useful in medicinal chemistry for const

Used as a chiral building block in the synthesis of biologically active molecules, particularly in the development of pharmaceuticals. Its protected amine and hydroxyl functionalities make it valuable in peptide-like structures and beta-amino alcohol synthesis. Commonly employed in asymmetric synthesis due to the stable chiral center, enabling selective formation of desired stereoisomers. The sulfonyl group enhances reactivity and directs selective transformations, useful in medicinal chemistry for constructing protease inhibitors or enzyme modulators.

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