N-Boc-azetidine-3-sulfonyl Chloride

≥95%

Reagent Code: #220333
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CAS Number 1310732-18-3

science Other reagents with same CAS 1310732-18-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 255.72 g/mol
Formula C₈H₁₄ClNO₄S
badge Registry Numbers
MDL Number MFCD11040529
inventory_2 Storage & Handling
Storage -20°C, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical development. Its structure allows for selective modification in drug design, making it valuable in creating protease inhibitors and other therapeutic agents. The sulfonyl chloride group readily reacts with nucleophiles such as amines or alcohols, enabling efficient formation of sulfonamides or sulfonate esters. The Boc-protected azetidine ring offers stability and controlled deprotection, useful in multi-step syntheses. Commonly applied in medicinal chemistry for constructing constrained ring systems that improve metabolic stability and binding affinity in drug candidates.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,290.00
inventory 250mg
10-20 days ฿12,960.00
inventory 1g
10-20 days ฿33,380.00
inventory 500mg
10-20 days ฿23,040.00
N-Boc-azetidine-3-sulfonyl Chloride
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Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical development. Its structure allows for selective modification in drug design, making it valuable in creating protease inhibitors and other therapeutic agents. The sulfonyl chloride group readily reacts with nucleophiles such as amines or alcohols, enabling efficient formation of sulfonamides or sulfonate esters. The Boc-protected azetidine ring offers stability and controlled deprotection, useful i

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical development. Its structure allows for selective modification in drug design, making it valuable in creating protease inhibitors and other therapeutic agents. The sulfonyl chloride group readily reacts with nucleophiles such as amines or alcohols, enabling efficient formation of sulfonamides or sulfonate esters. The Boc-protected azetidine ring offers stability and controlled deprotection, useful in multi-step syntheses. Commonly applied in medicinal chemistry for constructing constrained ring systems that improve metabolic stability and binding affinity in drug candidates.

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