4-(TOLUENE-4-SULFONYLOXY)-PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER

96%

Reagent Code: #240064
label
Alias 4-(Toluene-4-sulfonyloxy)piperidine-1-carboxylic acid tert-butyl ester
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CAS Number 118811-07-7

science Other reagents with same CAS 118811-07-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 355.45 g/mol
Formula C₁₇H₂₅NO₅S
badge Registry Numbers
MDL Number MFCD06796535
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) that require functionalized piperidine moieties. Its protected amine and activated hydroxyl group allow selective reactions in multi-step organic syntheses. Commonly employed in the preparation of kinase inhibitors, antiviral agents, and central nervous system modulators. Suitable for use in coupling reactions and nucleophilic substitutions due to the tosylate leaving group. The tert-butyl carbamate (Boc) protection ensures amine stability during reaction sequences, enabling deprotection under mild acidic conditions when needed.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿154.00
inventory 5g
10-20 days ฿170.50
inventory 25g
10-20 days ฿1,410.00
inventory 100g
10-20 days ฿5,120.00
4-(TOLUENE-4-SULFONYLOXY)-PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) that require functionalized piperidine moieties. Its protected amine and activated hydroxyl group allow selective reactions in multi-step organic syntheses. Commonly employed in the preparation of kinase inhibitors, antiviral agents, and central nervous system modulators. Suitable for use in coupling reactions and nucleophilic substitutions due to the tosylate

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) that require functionalized piperidine moieties. Its protected amine and activated hydroxyl group allow selective reactions in multi-step organic syntheses. Commonly employed in the preparation of kinase inhibitors, antiviral agents, and central nervous system modulators. Suitable for use in coupling reactions and nucleophilic substitutions due to the tosylate leaving group. The tert-butyl carbamate (Boc) protection ensures amine stability during reaction sequences, enabling deprotection under mild acidic conditions when needed.

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