tert-butyl 3-(4-methylphenyl)sulfonyloxypiperidine-1-carboxylate

≥98%

Reagent Code: #241034
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CAS Number 85275-46-3

science Other reagents with same CAS 85275-46-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 355.45 g/mol
Formula C₁₇H₂₅NO₅S
badge Registry Numbers
MDL Number MFCD07787194
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of selective receptor modulators. Its structure supports the construction of complex molecules with high stereochemical control, making it valuable in medicinal chemistry for creating drug candidates targeting neurological and psychiatric disorders. The tert-butoxycarbonyl (Boc) protecting group allows for controlled amine reactivity, while the sulfonyloxy moiety serves as a good leaving group in coupling reactions. Commonly employed in multi-step organic syntheses where functional group compatibility and stability are required.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿990.00
inventory 5g
10-20 days ฿4,940.00
inventory 25g
10-20 days ฿18,630.00
inventory 10g
10-20 days ฿9,190.00
tert-butyl 3-(4-methylphenyl)sulfonyloxypiperidine-1-carboxylate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of selective receptor modulators. Its structure supports the construction of complex molecules with high stereochemical control, making it valuable in medicinal chemistry for creating drug candidates targeting neurological and psychiatric disorders. The tert-butoxycarbonyl (Boc) protecting group allows for controlled amine reactivity, while the sulfonyloxy moiety serves as a good leaving group in couplin

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of selective receptor modulators. Its structure supports the construction of complex molecules with high stereochemical control, making it valuable in medicinal chemistry for creating drug candidates targeting neurological and psychiatric disorders. The tert-butoxycarbonyl (Boc) protecting group allows for controlled amine reactivity, while the sulfonyloxy moiety serves as a good leaving group in coupling reactions. Commonly employed in multi-step organic syntheses where functional group compatibility and stability are required.

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