(S)-Oxetan-2-ylmethanamine 4-methylbenzenesulfonate

98%

Reagent Code: #233683
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CAS Number 2740593-38-6

science Other reagents with same CAS 2740593-38-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 259.32 g/mol
Formula C₁₁H₁₇NO₄S
badge Registry Numbers
MDL Number MFCD34577559
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a chiral building block in pharmaceutical synthesis, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. The oxetane ring offers metabolic stability and improved physicochemical properties in drug candidates. Commonly employed in the preparation of protease inhibitors and kinase inhibitors due to its ability to mimic structural motifs in biologically active molecules. The tosylate group facilitates salt formation and enhances crystallinity, aiding in purification and isolation during multi-step syntheses. Also utilized in the manufacture of certain antiviral and anticancer agents where stereochemistry plays a critical role in efficacy.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,910.00
inventory 1g
10-20 days ฿3,870.00
inventory 5g
10-20 days ฿11,750.00
(S)-Oxetan-2-ylmethanamine 4-methylbenzenesulfonate
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Used as a chiral building block in pharmaceutical synthesis, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. The oxetane ring offers metabolic stability and improved physicochemical properties in drug candidates. Commonly employed in the preparation of protease inhibitors and kinase inhibitors due to its ability to mimic structural motifs in biologically active molecules. The tosylate group facilitates salt formation and enhances crystallinity,
Used as a chiral building block in pharmaceutical synthesis, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. The oxetane ring offers metabolic stability and improved physicochemical properties in drug candidates. Commonly employed in the preparation of protease inhibitors and kinase inhibitors due to its ability to mimic structural motifs in biologically active molecules. The tosylate group facilitates salt formation and enhances crystallinity, aiding in purification and isolation during multi-step syntheses. Also utilized in the manufacture of certain antiviral and anticancer agents where stereochemistry plays a critical role in efficacy.
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